戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 54724作成日:2026年10月26日

Acetic Acid → 3,4-Diacetoxy-1-butene

https://huagongshe.com/reaction/54724

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物TributylamineHCID 7622—
反応物Acetic AnhydrideHCID 7918—
反応物VinyloxiraneHCID 13586—
溶媒DiglymeHCID 8150—
生成物3,4-Diacetoxy-1-buteneHCID 273500179%

反応条件

温度125 °C

反応手順

A 300-mL autoclave was charged with 40 mL (0.50 mol) of 3,4-epoxy-1-butene, 60.0 g (0.59 mol) acetic anhydride, 3.7 g (0.02 mol) of tributylamine, 0.72 g (0.012 mol) acetic acid and 4.2 mL of diglyme. The autoclave was purged with nitrogen twice, then the vessel was pressurized to 8 bars (100 psig) with nitrogen. The agitator was started and an initial sample was taken. The mixture was heated to 125° C. During the course of 2 hrs, samples were taken every 15 min for analysis by GC. GC analysis of the crude mixture after 2 hrs revealed a 79% yield of 3,4-diacetoxy-1-butene with a 90% selectivity and 12% 3,4-epoxy-1-butene. The reaction was observed to be first order in 3,4-epoxy-1-butene with a first order rate constant of 0.017 min-1 (Table A). This example shows the catalytic effect of another tertiary amine with acetic acid as the co-catalyst.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05623086
出典データセットuspto-grants-1997_04
ORD IDord-3aa2160cfd7d48bfb175aee0e666131a
出典メモuspto-grants-1997_04