Acetic Acid → 1,3-Bis(3-bromophenyl)propan-2-ol

HRID 1160671ノート

反応式

HRID 1160671 の反応式
[BH4-].[Na+].[Br:3][C:4]1[CH:5]=[C:6]([CH:18]=[CH:19][CH:20]=1)[CH2:7][C:8]([CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([Br:17])[CH:12]=1)=[O:9].C(O)(C)C.C(O)(=O)C>C1COCC1>[Br:3][C:4]1[CH:5]=[C:6]([CH2:7][CH:8]([OH:9])[CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([Br:17])[CH:12]=2)[CH:18]=[CH:19][CH:20]=1

参加物

6

反応条件

温度
0 °C

実験手順

7.6 g (200 mmol) of sodium tetrahydridoborate were added at 0° C. to a solution of 36.8 g (100 mmol) of bis(3-bromobenzyl)ketone in a mixture of 500 ml of THF, 200 ml of isopropanol and 3 ml of acetic acid, and the mixture was stirred at 0° C. for a further 3 h. The ice bath was subsequently removed, and the mixture was stirred at room temperature for a further 12 h. After addition of 300 ml of saturated ammonium chloride solution, the organic phase was separated off, and the aqueous phase was extracted twice with 100 ml of dichloromethane. The combined organic phases were washed once with 500 ml of saturated sodium chloride solution and then freed from the solvent mixture in vacuo, giving 34.9 g (94 mmol), corresponding to 94.3% of theory, of the product in the form of an oil, 97% according to 1H-NMR, which were reacted further without purification.

後処理

  1. customThe ice bath was subsequently removed
  2. stirringthe mixture was stirred at room temperature for a further 12 h
  3. additionAfter addition of 300 ml of saturated ammonium chloride solution
  4. customthe organic phase was separated off
  5. extractionthe aqueous phase was extracted twice with 100 ml of dichloromethane
  6. washThe combined organic phases were washed once with 500 ml of saturated sodium chloride solution
  7. customgiving 34.9 g (94 mmol)
  8. customwere reacted further without purification

出典と根拠

ORDレコード
ord-c982db26f07d456a90b9c85701942b91
出典データセット
uspto-grants-2010_10
特許番号
US07816531B2

反応ノート

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