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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55601생성일: 2026년 10월 23일

Sodium borohydride → 4-(3-Chloropropoxy)-3-hydroxy-alpha-methylbenzenemethanol

https://huagongshe.com/ko/reaction/55601

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물1-(4-(3-Chloropropoxy)-3-hydroxyphenyl]ethanoneHCID 10376507—
용매Tetrahydrofuran ethanolHCID 21873804—
생성물4-(3-Chloropropoxy)-3-hydroxy-alpha-methylbenzenemethanolHCID 1039898655%

반응 조건

온도10 °C

반응 단계

To a flask charged with sodium borohydride (1.5 g, 39.4 mmol) under nitrogen and chilled to 10° C. was added, slowly, a solution of 1-[4-(3-chloropropoxy)-3-hydroxyphenyl]ethanone (6.0 g, 26.2 mmol) dissolved in ethanol-tetrahydrofuran (120 ml, 2:1). After total addition, the ice bath was removed and the reaction was stirred at ambient temperature for 3 hours. An additional amount of sodium borohydride (0.2 g, 5.3 mmol) was carefully added. After stirring at ambient temperature for one hour, the solvent was removed in vacuo. The resultant solid residue was diluted with water (100 ml) and left overnight. The product was isolated by vacuum filtration yielding 3.8 g. Two consecutive recrystallizations from toluene provided 3.3 g (55%) of 4-(3-chloropropoxy)-3-hydroxy-α-methylbenzene methanol as a light brown solid, m.p.=107°-109° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624927
출처 데이터셋uspto-grants-1997_04
ORD IDord-31eb0799bcf44dfc8bc8c8d6a7abf5b5
출처 메모uspto-grants-1997_04