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HRID 2415553생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/2415553

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 5085280385,587.203%

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 tetrahydrofuran (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 solution was cooled to approximately 0° C. and a solution of 1-(2-bromo-5-chlorophenyl)ethanone (3-3) (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 3-4 as a colorless solid (25.8 g; 98:2 S/R enantiomeric ratio).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06818658B2
출처 데이터셋uspto-grants-2004_11
ORD IDord-f1b6cf3d672c4854a0784922978c6683
출처 메모uspto-grants-2004_11