Ethanol → 2-(4-Bromo-2,6-dimethylphenoxy)ethanol

HRID 30754

반응식

HRID 30754 반응식
[BH4-].[Na+].[Br:3][C:4]1[CH:16]=[C:15]([CH3:17])[C:7]([O:8][CH2:9][C:10](OCC)=[O:11])=[C:6]([CH3:18])[CH:5]=1.O1CCCC1.C(O)C>O>[Br:3][C:4]1[CH:5]=[C:6]([CH3:18])[C:7]([O:8][CH2:9][CH2:10][OH:11])=[C:15]([CH3:17])[CH:16]=1

참가 물질

6

반응물 4

HCID 702EthanolHCID 8028TetrahydrofuranHCID 875019Ethyl (4-bromo-2,6-dimethylphenoxy)acetateHCID 4311764Sodium borohydride

생성물 1

HCID 537074432-(4-Bromo-2,6-dimethylphenoxy)ethanol수율 97.6%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Sodium borohydride (0.21 g) was added to a mixture of ethyl (4-bromo-2,6-dimethylphenoxy)acetate (0.78 g), tetrahydrofuran (5 mL) and ethanol (5 mL), and the mixture was stirred at room temperature for 4 hrs. The reaction mixture was diluted with water, and extracted with ethyl acetate. The organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent:ethyl acetate/n-hexane=1/2) to afford the title compound (0.65 g).

후처리

  1. extractionextracted with ethyl acetate
  2. washThe organic layer was washed with water and brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThe solvent was evaporated under reduced pressure
  5. customthe residue was purified by silica gel column chromatography (eluent:ethyl acetate/n-hexane=1/2)

출처 및 근거

ORD 기록
ord-63919e776b274c8f99d5d3eca09608aa
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07423185B2

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