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

HRID 2220631

反応式

HRID 2220631 の反応式
[BH4-].[Na+].C([O:5][C:6](=O)[CH2:7][O:8][C:9]1[C:14]([CH3:15])=[CH:13][C:12]([Br:16])=[CH:11][C:10]=1[CH3:17])C.O1CCCC1.C(O)C>O>[Br:16][C:12]1[CH:11]=[C:10]([CH3:17])[C:9]([O:8][CH2:7][CH2:6][OH:5])=[C:14]([CH3:15])[CH:13]=1

参加物

6

反応物 4

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

生成物 1

HCID 537074432-(4-Bromo-2,6-dimethylphenoxy)ethanol収率 96.6%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Sodium borohydride (0.206 g) was added to a mixture of ethyl(4-bromo-2,6-dimethylphenoxy)acetate (0.782 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 (0.645 g).

後処理

  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)

出典と根拠

ORDレコード
ord-39dba05a1b9b441197d4fa26af2ce661
出典データセット
uspto-grants-2008_08
特許番号
US07417169B2

関連ノート

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