돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6435생성일: 2026년 10월 24일

Phenol → (2,2-Diethoxyethoxy)benzene

https://huagongshe.com/ko/reaction/6435

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물Sodium hydrideHCID 24758—
반응물Ethane, 2-bromo-1,1-diethoxy-HCID 74852—
용매2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
생성물(2,2-Diethoxyethoxy)benzeneHCID 96328—

반응 조건

온도110 °C

반응 단계

Sodium hydride (5.83 g of a 55% dispersion in mineral oil) was added to a solution of phenol (12.56 g) in DMPU (25 ml) at 5° C. and the mixture was stirred for 30 minutes. Bromoacetaldehyde diethyl acetal (10.05 ml) was added and the mixture was heated at 110° C. for 5 hours, then allowed to cool. The mixture was partitioned between ethyl acetate (100 ml) and water (100 ml) and the organic phase was separated and washed sequentially with aqueous 2M sodium hydroxide solution (2×50 ml) and water (50 ml). The aqueous fractions were combined and re-extracted with ethyl acetate (100 ml). The combined organic extracts were dried (MgSO4) and concentrated. The resultant oil was purified by flash column chromatography, eluting with ethyl acetate/hexane (1:10 v/v) to give 2-phenoxyacetaldehyde diethyl acetal (9.43 g) as an oil; NMR: 1.25(6H,t, J=7.0 Hz), 3.6-3.85(4H,m), 4.05(2 H,d, J=6.0 Hz), 4.85 (1H,t, J=6.0 Hz) and 6.9-7.35(5H,m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248780
출처 데이터셋uspto-grants-1993_09
ORD IDord-db8a01301d8543ea840e78a021d649d8
출처 메모uspto-grants-1993_09