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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400234생성일: 2026년 10월 26일

p-Toluenesulfonic acid → Oxiranemethanol, 3-[(phenylmethoxy)methyl]-

https://huagongshe.com/reaction/400234

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물2,2-DimethoxypropaneHCID 6495—
반응물1,4-DioxaneHCID 31275—
용매AcetoneHCID 180—
용매Diethyl EtherHCID 3283—
생성물Oxiranemethanol, 3-[(phenylmethoxy)methyl]-HCID 3934498—

반응 단계

2,2-Dimethoxypropane (12 mL, 97 mmol) was added with stirring to a solution of crude diols A and B, catalytic p-toluenesulfonic acid in acetone (50 mL). The mixture was stirred at room temperature overnight, diluted with ether and washed with aqueous sodium bicarbonate solution (twice). The organic extract was dried (magnesium sulfate), filtered and concentrated. The crude oil was chromatographed on a silica gel column and eluted with 2-10% ethyl acetate in hexanes to obtain dioxane C (5.85 g, 65% overall yield from 4-benzyloxy-2,3-epoxy-1-butanol) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05827868
출처 데이터셋uspto-grants-1998_10
ORD IDord-ede2c44152fa49799c2be5af1e02fafb
출처 메모uspto-grants-1998_10