反応式
[C:1]([OH:7])(=[O:6])[C:2]([CH3:5])([CH3:4])[CH3:3].[C]=O.[C:10](OC=C)(=O)[CH3:11]>[Ru]>[C:1]([O:7][CH:10]=[CH2:11])(=[O:6])[C:2]([CH3:5])([CH3:4])[CH3:3]参加物
実験手順
Vinyl pivalate (91 pounds) was prepared in two, 20 gallon-batch runs in a 30 gallon stainless steel reactor. In two batches, pivalic acid (75.5 lbs, 10 gallons) and vinyl acetate (77.9 lbs, 10 gallons) were transvinylated in the presence of 300 ppm ruthenium catalyst, described in the preceeding paragraph, at 145° C. using a 50 psig carbon monoxide reaction atmosphere for 5 hours. Reaction product was removed from the reactor by vacuum distillation (60°-130° C., 240 mm Hg) from the ruthenium catalyst without difficulty. Based on gas chromatographic analysis, 90.4% and 94.7% of the vinyl pivalate respectively formed in the two reaction batches, could be accounted for after distillation. This demonstrates that reequilibration of vinyl pivalate (and acetic acid) to vinyl acetate (and pivalic acid) was successfully controlled during distillation within 9.6% (batch 1) and 5.3% (batch 2), respectively. Mass balances for all components were better than 98%.
後処理
- customdescribed in the preceeding paragraph, at 145° C.
- customReaction product
- customwas removed from the reactor by vacuum distillation (60°-130° C., 240 mm Hg) from the ruthenium catalyst without difficulty
- customrespectively formed in the two reaction batches
- distillationafter distillation
- distillationwas successfully controlled during distillation within 9.6% (batch 1) and 5.3% (batch 2)
出典と根拠
- ORDレコード
- ord-38bd47a1211b4096b53988f3286e4c2f
- 出典データセット
- uspto-grants-1991_01
- 特許番号
- US04981973
関連ノート
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