Methanol → 5-Bromo-2-methyl-2-phenylpentan-1-ol

HRID 47991

반응식

HRID 47991 반응식
CO.[Li+].[BH4-].[Br:5][CH2:6][CH2:7][CH2:8][C:9]([CH3:21])([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:10](OCC)=[O:11].[NH4+].[Cl-]>C(Cl)Cl>[Br:5][CH2:6][CH2:7][CH2:8][C:9]([CH3:21])([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[CH2:10][OH:11]

참가 물질

6

실험 절차

Methanol (5.24 g, 164 mmol) was added drop-wise to a stirred suspension of LiBH4 (3.45 g, 150 mmol) in anhydrous CH2Cl2 (150 mL) under N2 atmosphere. After the addition of ethyl 5-bromo-2-methyl-2-phenyl-pentanoate (23.70 g, 106 mmol), the reaction mixture was heated to reflux overnight. The reaction mixture was cooled to 5° C. and hydrolyzed with ice (ca. 30 g) and NH4Cl solution (150 mL) for 1 h. The layers were separated and the aqueous layer was extracted with CH2Cl2 (3×150 mL). The combined organic layers were washed with NH4Cl solution (3×100 mL), dried over MgSO4 and concentrated in vacuo to furnish 5-bromo-2-methyl-2-phenyl-pentan-1-ol (20 g, 96.8%) as an oil. 1H NMR (300 MHz, CDCl3/TMS): δ (ppm) 7.34-7.14 (m, 5H), 3.60 (m, 1H), 3.48 (m, 1H), 3.29 (t, J=6.0 Hz, 2H), 1.96-1.44 (m, 5H), 1.32 (s, 3H). 13C NMR (75 MHz, CDCl3/TMS): δ (ppm) 144.25, 128.59, 126.71, 126.41, 72.44, 43.15, 37.06, 34.64, 27.58, 21.61. HRMS (LSIMS, nba): Calcd. for C2H16Br (MH+—H2O): 239.0435, found: 239.0444.

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureto reflux overnight
  3. customThe layers were separated
  4. extractionthe aqueous layer was extracted with CH2Cl2 (3×150 mL)
  5. washThe combined organic layers were washed with NH4Cl solution (3×100 mL)
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-11a0224e549043658adeb941c3c5cc96
출처 데이터셋
uspto-grants-2004_03
특허 번호
US06699910B2

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