돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34833생성일: 2026년 10월 24일

Bromo(phenyl)acetic acid → 2-Bromo-2-phenylethanol

https://huagongshe.com/ko/reaction/34833

반응식

참여 물질

역할이름HCID투입량
반응물Bromo(phenyl)acetic acidHCID 97919—
반응물DiboronHCID 6328200—
반응물Oxolane--water (1/1)HCID 21881883—
용매TetrahydrofuranHCID 8028—
생성물2-Bromo-2-phenylethanolHCID 578332—

반응 단계

To a stirred solution of 25 g of α-bromphenylacetic acid in 100 ml of dry tetrahydrofuran was added 151 ml of 1.0M diborane in tetrahydrofuran dropwise at 5° C. under argon over 30 minutes. This mixture was stirred overnight at room temperature, then cooled to 0° C. and 130 ml of tetrahydrofuran:water (1:1) was added dropwise. The mixture was then saturated with potassium carbonate and the tetrahydrofuran removed. The aqueous remainder was extracted three times with ether. The extracts were combined and dried. The residue was triturated with hexane and the solid collected giving the desired compound as white needles, mp 38°-39° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04762942
출처 데이터셋uspto-grants-1988_08
ORD IDord-b0f3831dca3c442fb30e53f98498613d
출처 메모uspto-grants-1988_08