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HRID 54722作成日:2026年10月26日

Acetic Anhydride → 3,4-Diacetoxy-1-butene

https://huagongshe.com/reaction/54722

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物DiglymeHCID 8150—
反応物TriethylamineHCID 8471—
反応物VinyloxiraneHCID 13586—
生成物3,4-Diacetoxy-1-buteneHCID 273500192%

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, 63.2 g (0.62 mol) acetic anhydride, 4.06 g (0.041 mol) of triethylamine 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 2.5 hrs, samples were taken every 15 min for analysis by GC. GC analysis of the crude mixture after 2.5 hrs revealed a 92% yield of 3,4-diacetoxy-1-butene with a 92% selectivity and 0.36% 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 0.037 min-1 (Table A). This example demonstrates the catalytic effect of the tertiary amine alone.

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-6e6ef29129cb420f913406ea274eb835
出典メモuspto-grants-1997_04