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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 743378생성일: 2026년 10월 25일

Salicyl Alcohol → Benzenemethanol, 2-(phenylmethoxy)-

https://huagongshe.com/reaction/743378

반응식

참여 물질

역할이름HCID투입량
반응물Salicyl AlcoholHCID 5146—
반응물Benzyl BromideHCID 7498—
반응물HexaneHCID 8058—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물Benzenemethanol, 2-(phenylmethoxy)-HCID 1881187%

반응 단계

151 g of potassium t-butoxide were added, whilst ice-cooling and stirring, to a solution of 152 g of salicyl alcohol in 600 ml of dimethylformamide, and the resulting mixture was stirred at room temperature for 30 minutes; 160 ml of benzyl bromide were then added dropwise to the mixture. The reaction mixture was then stirred at a temperature of from 30° to 40° C. for 2 hours, after which it was partitioned between ethyl acetate and water. The organic layer was washed twice, each time with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and concentrated by evaporation under reduced pressure. The oily residue thus obtained was subjected to column chromatography through silica gel, using a 5:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 228.5 g (yield 87%) of 2-benzyloxybenzyl alcohol as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05556864
출처 데이터셋uspto-grants-1996_09
ORD IDord-ca8ed899893e4c4988b0ee3b61efe071
출처 메모uspto-grants-1996_09