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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5901생성일: 2026년 10월 25일

Acetone → (2-(Benzyloxy)-3-methoxyphenyl)methanol

https://huagongshe.com/reaction/5901

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물2-(Benzyloxy)-3-methoxybenzaldehydeHCID 1268087—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
생성물(2-(Benzyloxy)-3-methoxyphenyl)methanolHCID 92725086%

반응 단계

A solution of 43.00 g (0.18 mole) of 2-benzyloxy-3-methoxy-benzaldehyde of Example 1 in 300 mL of absolute ethanol is treated, with stirring, with 7.56 g (0.20 mole) of sodium borohydride. The temperature rises to 50° C. After one-half hour 10 mL of acetone is added, keeping the temperature at less than 60° C. with cooling. After 15 minutes the volatiles are stripped off at reduced pressure. Ice water (500 mL) is added and the product is extracted into 600 mL of ethyl acetate. The dried (Na2SO4) solution is concentrated. The remaining oil is dissolved in 100 mL of warm ether. Petroleum ether is added to turbidity to give 37.70 g (86% yield) of pure product; mp 58°-60° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246943
출처 데이터셋uspto-grants-1993_09
ORD IDord-27c222d747194cee97fae27c69eb7117
출처 메모uspto-grants-1993_09