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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400233생성일: 2026년 10월 25일

Oxiranemethanol, 3-[(phenylmethoxy)methyl]- → 3-Allyl-4-(benzyloxy)-3-hydroxy-1-butanol

https://huagongshe.com/reaction/400233

반응식

참여 물질

역할이름HCID투입량
반응물Oxiranemethanol, 3-[(phenylmethoxy)methyl]-HCID 3934498—
반응물HCID 178418473HCID 178418473—
용매TetrahydrofuranHCID 8028—
생성물3-Allyl-4-(benzyloxy)-3-hydroxy-1-butanolHCID 18944106—

반응 조건

온도-40 °C

반응 단계

A solution of 4-benzyloxy-2,3-epoxy-1-butanol (6.28 g, 32.37 mmol) in anhydrous tetrahydrofuran (75 mL) was added dropwise at -40° C. over a period of 45 minutes, to a 2M solution of allyl magnesium chloride (48.5 mL, 97 mmol) and tetrahydrofuran (50 mL). The solution was stirred at -40° C. for 1 hour, warmed to 0° C. and quenched by addition of aqueous ammonium chloride solution. The tetrahydrofuran layer was separated and the aqueous layer was extracted with ethyl acetate (three times). The combined organic extract was dried (magnesium sulfate), filtered and concentrated to obtain a mixture of compounds A and B.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05827868
출처 데이터셋uspto-grants-1998_10
ORD IDord-757e5a1c8b554ab7918a14250606dd48
출처 메모uspto-grants-1998_10