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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1595511생성일: 2026년 10월 26일

Diethyl Ether → Benzeneethanol, 4-(acetyloxy)-

https://huagongshe.com/reaction/1595511

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물Acetic AnhydrideHCID 7918—
반응물TyrosolHCID 10393—
반응물Potassium HydroxideHCID 14797—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Benzeneethanol, 4-(acetyloxy)-HCID 58667667%

반응 단계

5.6 g (0.1 mole) potassium hydroxide in 10 ml water was added to a cooled solution of 13.8 g (0.1 mole) p-hydroxyphenethyl alcohol in 50 ml tetrahydrofuran. 10.2 g (0.1 mole) acetic anhydride was slowly added under stirring. After 2 hours diethyl ether and water were added. The phases were separated and the organic phase was dried, filtered and evaporated in vacuo. The product contained 15% starting material and was therefore redissolved in diethyl ether and washed twice with dilute sodium carbonate. Drying, filtration and evaporation of solvents in vacuo gave 12 g (yield 67%) of 2-(4-methylcarbonyloxyphenyl)-1-ethanol which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06288096B1
출처 데이터셋uspto-grants-2001_09
ORD IDord-ecd20afd2ef34717a3827cdc48a36da5
출처 메모uspto-grants-2001_09