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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227895생성일: 2026년 10월 25일

Chlorobis(2,6,6-trimethylbicyclo(3.1.1)heptan-3-yl)borane → (R)-1-(2',4'-dichloro-biphenyl-4-yl)-hex-5-en-1-ol

https://huagongshe.com/reaction/227895

반응식

참여 물질

역할이름HCID투입량
반응물Chlorobis(2,6,6-trimethylbicyclo(3.1.1)heptan-3-yl)boraneHCID 13515837—
반응물1-(2',4'-Dichloro-biphenyl-4-yl)-hex-5-en-1-oneHCID 57757263—
용매Diethyl EtherHCID 3283—
생성물(R)-1-(2',4'-dichloro-biphenyl-4-yl)-hex-5-en-1-olHCID 57757255—

반응 단계

(+)DIP-Chloride (2.4 g) was dissolved in dry ether (10 mL) and cooled in an ethanol/CO2 bath. 1-(2′,4′-Dichloro-biphenyl-4-yl)-hex-5-en-1-one (1 g) was dissolved in dry ether (5 mL) and added dropwise to the DIP solution. The mixture was allowed to warm to room temperature and stirred for 24 hours. Petrol (50 mL) was added and the organic layer was separated. The aqueous layer was diluted with water and extracted with a further 50 mL petrol. The organics were combined, dried and evaporated to give a thick oil. It was not possible to obtain a pure sample by column chromatography, but no trace of starting material remained, as assessed by thin layer chromatography.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560597B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-069bb6ea66c24220a267c07d54ed877e
출처 메모uspto-grants-2009_07