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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7849생성일: 2026년 10월 23일

Boron tribromide → 9a-BUTYL-7-HYDROXY-8-METHYL-1,2,9,9a-TETRAHYDRO-3H-FLUOREN-3-ONE

https://huagongshe.com/ko/reaction/7849

반응식

참여 물질

역할이름HCID투입량
반응물Boron tribromideHCID 25134—
반응물9a-butyl-7-methoxy-8-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-oneHCID 21990884—
용매DichloromethaneHCID 6344—
생성물9a-BUTYL-7-HYDROXY-8-METHYL-1,2,9,9a-TETRAHYDRO-3H-FLUOREN-3-ONEHCID 996527299.1%

반응 단계

A solution of 9a-butyl-7-methoxy-8-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (28.4 mg, 0.1 mmol) in anhydrous CH2Cl2 (1.7 mL) was stirred under a nitrogen atmosphere and cooled in a dry ice-acetone bath while 1M BBr3 in CH2Cl2 (0.30 mL, 0.3 mmol) was added dropwise by syringe. The cooling bath was removed and the reaction mixture was stirred at room temperature for 4 hours. The mixture was diluted with EtOAc (8 mL), water (3 mL) and 1N HCL (1 mL) and shaken vigorously. The EtOAc layer was separated, washed with water (3 mL), 1M pH 3 phosphate (3 mL) and brine (3 mL), dried over MgSO4, filtered and evaporated under vacuum to give an ochre solid (26.8 mg). The crude product was suspended in CDCl3 (1 mL) and filtered. The solid portion was dried under vacuum to afford 9a-butyl-7-hydroxy-8-methyl-1,2,9,9a-3H-tetrahydro-fluoren-3-one as an olive colored powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087599B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-a3003665ff944b9aba117505583cfbac
출처 메모uspto-grants-2006_08