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Sodium borohydride → 1-(3-Bromo-2-methylphenyl)-1-pentanol

HRID 1391794
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HRID 1391794 반응식
[Br:1][C:2]1[C:3]([CH3:14])=[C:4]([C:8](=[O:13])[CH2:9][CH2:10][CH2:11][CH3:12])[CH:5]=[CH:6][CH:7]=1.[BH4-].[Na+]>C1COCC1.O>[Br:1][C:2]1[C:3]([CH3:14])=[C:4]([CH:8]([OH:13])[CH2:9][CH2:10][CH2:11][CH3:12])[CH:5]=[CH:6][CH:7]=1
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참가 물질

5

반응물 2

HCID 4311764Sodium borohydride2회HCID 586298971-(3-Bromo-2-methylphenyl)-1-pentanone

생성물 1

HCID 586298181-(3-Bromo-2-methylphenyl)-1-pentanol수율 69.5%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

To a solution of 1-(3-bromo-2-methylphenyl)-1-pentanone (706 mg, 2.77 mmol) in anhydrous THF (12 mL) under nitrogen at 0° C. was added sodium borohydride (209 mg, 5.53 mmol) in water (8 mL) and the resulting mixture stirred at 0° C. for 2 h. Additional sodium borohydride (105 mg, 2.77 mmol) was then added, along with more THF (40 mL), and the resulting mixture stirred at 0° C. for an additional 30 min. The reaction mixture was then partitioned between EtOAc (50 mL) and water (50 mL), the layers separated, and the aqueous re-extracted with EtOAc (50 mL). The combined organic solution was then dried (Na2SO4) filtered, and reduced under vacuum. Purification by SPE (silica, 20 g cartridge), eluted with cyclohexane:EtOAc (gradient 99:1 to 19:1) afforded the title compound as a colourless oil (495 mg).

후처리

  1. stirringthe resulting mixture stirred at 0° C. for an additional 30 min
  2. customThe reaction mixture was then partitioned between EtOAc (50 mL) and water (50 mL)
  3. customthe layers separated
  4. extractionthe aqueous re-extracted with EtOAc (50 mL)
  5. dry with materialThe combined organic solution was then dried (Na2SO4)
  6. filtrationfiltered
  7. customPurification by SPE (silica, 20 g cartridge)
  8. washeluted with cyclohexane

출처 및 근거

ORD 기록
ord-f50e7d2fc4554ab89dc2dab9d1ad606c
출처 데이터셋
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07338960B2

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