| Aspects of Homogeneous Catalysis: Vol. IV Softcover Repri Edition Contributor(s): Ugo, R. (Editor) |
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ISBN: 9400983735 ISBN-13: 9789400983731 Publisher: Springer OUR PRICE: $52.24 Product Type: Paperback - Other Formats Published: October 2011 |
| Additional Information |
| BISAC Categories: - Science | Chemistry - Industrial & Technical - Science | Chemistry - Physical & Theoretical - Technology & Engineering | Materials Science - General |
| Dewey: 541 |
| Series: Aspects of Homogeneous Catalysis |
| Physical Information: 0.46" H x 6.69" W x 9.61" (0.77 lbs) 212 pages |
| Descriptions, Reviews, Etc. |
| Publisher Description: Another approach is via the peracid route 10, Il], whereby propylene is epoxidized by an organic peracid, usually peracetic acid. The latter is prepared either by reaction of acetic acid with hydrogen peroxide, or by autoxidation of acetaldehyde. - (3) - (4) ---I.... MeC0 H MeCHO +02 3 /'\. (5) MeC0 H + MeCH=CH ---I .... MeCH-CH + MeC0 H 3 2 2 2 Although this method has been extensively studied 10, II] and is often the method of choice for laboratory scale preparations of epoxides, it has not been widely applied on a commercial scale. The reasons are probably to be found in the hazards associated with the handling of these explosive and corrosive peracids on an industrial scale. Nevertheless, several companies continue to groom this method for future commercialization 12]. With organic hydroperoxides becoming available as commercial chemicals, in the last decade propylene oxide process technology has seen the commercializa- tion of the hydroperoxide route. Such a process, developed by Halcon Interna- tional and Atlantic Richfield, is that often referred to as the Halcon or Oxirane process 13]. It involves the reaction of propylene with an alkyl hydroperoxide in the presence of a soluble, metal catalyst (usually a molybdenum compound). The alkyl hydroperoxide is prepared by autoxidation of an appropriate hydro- carbon. For example, tert-butyl hydroperoxide (TBHP) is prepared by autoxida- tion of isobutane. (6) Reaction with propylene gives propylene oxide and tert-butanol as a coproduct. |