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Monsanto process

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and methyl iodide, which in turn affords, through carbonylation, acetyl iodide. Acetyl iodide reacts with acetate salts or acetic acid to give the anhydride. Rhodium iodides and lithium salts are employed as catalysts. Because acetic anhydride hydrolyzes, the conversion is conducted under anhydrous
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Zoeller, J. R.; Agreda, V. H.; Cook, S. L.; Lafferty, N. L.; Polichnowski, S. W.; Pond, D. M. (1992). "Eastman Chemical Company Acetic Anhydride Process".
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in a process that is similar to the Monsanto acetic acid synthesis. Methyl acetate is used in place of methanol as a source of methyl iodide.
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Hartwig, J. F. Organotransition Metal Chemistry, from Bonding to Catalysis; University Science Books: New York, 2010.
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of 150–200 Â°C and gives a selectivity greater than 99%. It was developed in 1960 by the German chemical company
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https://web.archive.org/web/20050412040850/http://www.uyseg.org/catalysis/ethacid/ethacid2.htm
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involves two non-organometallic steps: conversion of methanol to
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Hosea Cheung, Robin S. Tanke, G. Paul Torrence "Acetic Acid" in
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to form the six-coordinate dicarbonyl complex, which undergoes
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conditions in contrast to the Monsanto acetic acid synthesis.
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Arene complexes of univalent gallium, indium, and thallium
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complex . This five-coordinate complex then reacts with
344:"The Cativa Process for the Manufacture of Acetic Acid" 700: 654: 558: 522: 451: 128:species . This anion rapidly transforms, via the 81:in 1966, which introduced a new catalyst system. 34:is an industrial method for the manufacture of 267:Ullmann's Encyclopedia of Industrial Chemistry 186:with respect to methyl iodide and . Hence the 429: 8: 93:The catalytic cycle of the Monsanto process 530:Oxidative addition / reductive elimination 436: 422: 414: 294:. Archived from the original on 2014-08-11 198:Tennessee Eastman acetic anhydride process 288:"Production method: The Monsanto process" 27:Method for the manufacture of acetic acid 479:Polyhedral skeletal electron pair theory 258: 304: 7: 586:Transition metal fullerene complexes 190:of methyl iodide is proposed as the 621:Transition metal carbyne complexes 616:Transition metal carbene complexes 581:Transition metal indenyl complexes 182:The reaction has been shown to be 25: 631:Transition metal alkyne complexes 626:Transition metal alkene complexes 636:Transition-metal allyl complexes 143:, affording the pentacoordinate 611:Transition metal acyl complexes 18:Monsanto acetic acid synthesis 1: 269:, 2002, Wiley-VCH, Weinheim. 108:- (top of scheme). The first 393:10.1016/0920-5861(92)80188-S 54:-based process developed by 687:Shell higher olefin process 494:Dewar–Chatt–Duncanson model 292:www.greener-industry.org.uk 245:converts methyl acetate to 61:This process operates at a 778: 576:Cyclopentadienyl complexes 540:β-hydride elimination 514:Metal–ligand multiple bond 364:10.1595/003214000X44394105 171:and the hydrolysis of the 641:Transition metal carbides 311:: CS1 maint: unfit URL ( 742:Organometallic chemistry 445:Organometallic chemistry 275:10.1002/14356007.a01_045 606:Half sandwich compounds 721:Bioinorganic chemistry 101:active species is the 94: 692:Ziegler–Natta process 596:Metal tetranorbornyls 342:Jones, J. H. (2000). 192:rate-determining step 179:and hydrogen iodide. 153:reductive elimination 136:group to an adjacent 92: 701:Related branches of 459:Crystal field theory 352:Platinum Metals Rev. 77:and improved by the 716:Inorganic chemistry 535:Migratory insertion 509:Agostic interaction 464:Ligand field theory 757:Chemical processes 601:Sandwich compounds 559:Types of compounds 484:Isolobal principle 188:oxidative addition 114:oxidative addition 95: 729: 728: 711:Organic chemistry 682:Olefin metathesis 672:Grignard reaction 571:Grignard reagents 16:(Redirected from 769: 677:Monsanto process 474:d electron count 469:18-electron rule 438: 431: 424: 415: 397: 396: 374: 368: 367: 348: 339: 333: 323: 317: 316: 310: 302: 300: 299: 284: 278: 263: 241:In this process 203:Acetic anhydride 79:Monsanto Company 56:BP Chemicals Ltd 32:Monsanto process 21: 777: 776: 772: 771: 770: 768: 767: 766: 732: 731: 730: 725: 696: 650: 566:Gilman reagents 554: 550:Carbometalation 545:Transmetalation 518: 447: 442: 405: 400: 380:Catalysis Today 376: 375: 371: 346: 341: 340: 336: 324: 320: 303: 297: 295: 286: 285: 281: 264: 260: 256: 247:lithium acetate 236: 232: 228: 224: 220: 205:is produced by 200: 165:catalytic cycle 162: 149:carbon monoxide 87: 85:Catalytic cycle 28: 23: 22: 15: 12: 11: 5: 775: 773: 765: 764: 759: 754: 749: 744: 734: 733: 727: 726: 724: 723: 718: 713: 707: 705: 698: 697: 695: 694: 689: 684: 679: 674: 669: 667:Cativa process 664: 658: 656: 652: 651: 649: 648: 643: 638: 633: 628: 623: 618: 613: 608: 603: 598: 593: 588: 583: 578: 573: 568: 562: 560: 556: 555: 553: 552: 547: 542: 537: 532: 526: 524: 520: 519: 517: 516: 511: 506: 501: 496: 491: 486: 481: 476: 471: 466: 461: 455: 453: 449: 448: 443: 441: 440: 433: 426: 418: 412: 411: 404: 403:External links 401: 399: 398: 369: 334: 318: 279: 257: 255: 252: 243:lithium iodide 239: 238: 234: 230: 226: 222: 218: 211:methyl acetate 199: 196: 160: 126:hexacoordinate 124:- to form the 110:organometallic 86: 83: 48:Cativa process 26: 24: 14: 13: 10: 9: 6: 4: 3: 2: 774: 763: 760: 758: 755: 753: 750: 748: 745: 743: 740: 739: 737: 722: 719: 717: 714: 712: 709: 708: 706: 704: 699: 693: 690: 688: 685: 683: 680: 678: 675: 673: 670: 668: 665: 663: 662:Carbonylation 660: 659: 657: 653: 647: 644: 642: 639: 637: 634: 632: 629: 627: 624: 622: 619: 617: 614: 612: 609: 607: 604: 602: 599: 597: 594: 592: 589: 587: 584: 582: 579: 577: 574: 572: 569: 567: 564: 563: 561: 557: 551: 548: 546: 543: 541: 538: 536: 533: 531: 528: 527: 525: 521: 515: 512: 510: 507: 505: 502: 500: 497: 495: 492: 490: 489:Ď€ backbonding 487: 485: 482: 480: 477: 475: 472: 470: 467: 465: 462: 460: 457: 456: 454: 450: 446: 439: 434: 432: 427: 425: 420: 419: 416: 410: 407: 406: 402: 394: 390: 386: 382: 381: 373: 370: 365: 361: 358:(3): 94–105. 357: 354: 353: 345: 338: 335: 332: 328: 322: 319: 314: 308: 293: 289: 283: 280: 276: 272: 268: 262: 259: 253: 251: 248: 244: 229:+ CO → (CH 216: 215: 214: 212: 208: 207:carbonylation 204: 197: 195: 193: 189: 185: 180: 178: 174: 173:acetyl iodide 170: 169:methyl iodide 166: 158: 157:acetyl iodide 154: 150: 146: 142: 139: 135: 131: 127: 123: 119: 118:methyl iodide 115: 111: 107: 104: 100: 99:catalytically 91: 84: 82: 80: 76: 72: 68: 64: 59: 57: 53: 49: 45: 41: 40:carbonylation 38:by catalytic 37: 33: 19: 676: 655:Applications 591:Metallocenes 387:(1): 73–91. 384: 378: 372: 355: 350: 337: 321: 296:. Retrieved 291: 282: 266: 261: 240: 201: 181: 163:C(O)I). The 121: 112:step is the 105: 96: 60: 50:, a similar 31: 29: 504:spin states 184:first-order 177:acetic acid 155:to release 71:temperature 36:acetic acid 736:Categories 452:Principles 331:189138953X 298:2014-08-27 254:References 752:Catalysis 703:chemistry 523:Reactions 499:Hapticity 130:migration 65:of 30–60 762:Monsanto 307:cite web 138:carbonyl 63:pressure 44:methanol 747:Rhodium 52:iridium 329:  145:acetyl 141:ligand 134:methyl 69:and a 347:(PDF) 132:of a 103:anion 327:ISBN 313:link 97:The 75:BASF 30:The 389:doi 360:doi 271:doi 233:CO) 209:of 175:to 159:(CH 122:cis 120:to 116:of 106:cis 67:atm 42:of 738:: 385:13 383:. 356:44 349:. 309:}} 305:{{ 290:. 225:CH 221:CO 217:CH 194:. 437:e 430:t 423:v 395:. 391:: 366:. 362:: 315:) 301:. 277:. 273:: 237:O 235:2 231:3 227:3 223:2 219:3 161:3 20:)

Index

Monsanto acetic acid synthesis
acetic acid
carbonylation
methanol
Cativa process
iridium
BP Chemicals Ltd
pressure
atm
temperature
BASF
Monsanto Company
The catalytic cycle of the Monsanto process
catalytically
anion
organometallic
oxidative addition
methyl iodide
hexacoordinate
migration
methyl
carbonyl
ligand
acetyl
carbon monoxide
reductive elimination
acetyl iodide
catalytic cycle
methyl iodide
acetyl iodide

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