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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31112생성일: 2026년 10월 26일

Water → 3-Benzyloxy-4-hydroxybenzaldehyde

https://huagongshe.com/reaction/31112

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Benzyl ChlorideHCID 7503—
반응물3,4-DihydroxybenzaldehydeHCID 8768—
반응물Sodium hydrideHCID 24758—
용매DimethylformamideHCID 6228—
생성물3-Benzyloxy-4-hydroxybenzaldehydeHCID 11020635—

반응 단계

Under atmosphere of argon, to a suspension of sodium hydride (63%, 57.1 g) in anhydrous N,N-dimethylformamide (540 ml) was added a solution of 3,4-dihydroxybenzaldehyde (103.5 g) in anhydrous N,N-dimethylformamide (500 ml) dropwise slowly under cooling with ice. The reaction mixture was stirred for 30 minutes at room temperature, and to the mixture was added benzyl chloride (104 ml) under cooling with ice and it was stirred for 15 hours at room temperature. To the mixture was added water under cooling with ice, and was concentrated under reduced pressure. The residue was diluted by water and it was washed by methylene chloride. The methylene chloride layer was extracted by a 1N aqueous solution of sodium hydroxide. Combined aqueous layers were acidified by 2M hydrochloric acid and it was extracted by ethyl acetate. The organic layer was washed by a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate and concentrated. The residue was recrystallized from chloroform to give the title compound (99.4 g) having the following physical data.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425567B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-569c2eeea7344c388f2fc4138da0f71c
출처 메모uspto-grants-2008_09