돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 644951생성일: 2026년 10월 23일

Trimethyl borate → (alphaR)-2-Bromo-5-chloro-alpha-methylbenzenemethanol

https://huagongshe.com/ko/reaction/644951

반응식

참여 물질

역할이름HCID투입량
반응물Trimethyl borateHCID 8470—
반응물2-Pyrrolidinemethanol, alpha,alpha-diphenyl-, (S)-HCID 2724899—
반응물1-(2-Bromo-5-chlorophenyl)ethanoneHCID 12486617—
용매TetrahydrofuranHCID 8028—
생성물(alphaR)-2-Bromo-5-chloro-alpha-methylbenzenemethanolHCID 50852803—

반응 조건

온도0 °C

반응 단계

Trimethylborate (1.74 mL, 15.4 mmol) was added to a stirred solution of (S)-(−)-alpha,alpha-diphenyl-2-pyrrolidinemethanol (3.24 g, 12.8 mol) in tetrahydrofaran (350 mL) at room temperature. After 1.25 h, borane-methyl sulfide complex (70.4 mL of a 2M solution in tetrahydrofuran, 0.141 mol) was added slowly and a gentle effervesence was observed. The resulting soution was cooled to approximately 0° C. and a solution of 1-(2-bromo-5-chlorophenyl)ethanone (˜30.0 g, 0.128 mmol) in tetrahydrofuran (150 mL) was then added uniformly over 1 h. After the addition, the resulting mixture was allowed to warm to ambient temperature and aged overnight. The reaction mixture was concentrated under reduced pressure to approximately one quarter of its original volume, poured into 1N hydrochloric acid and extracted three times with ethyl acetate. The combined organic extracts were washed with brine, dried (MgSO4) and concentrated in vacuo. Purification of the crude residue by flash chromatography on silica gel (9% ethyl acetate/hexanes as eluent) afforded the title compound as a colorless solid (98:2 enantiomer ratio).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07700778B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-15b34e9762014b7f966ed7ebc5d8bf02
출처 메모uspto-grants-2010_04