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

HRID 1160671노트

반응식

HRID 1160671 반응식
[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

참가 물질

6

반응 조건

온도
0 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-c982db26f07d456a90b9c85701942b91
출처 데이터셋
uspto-grants-2010_10
특허 번호
US07816531B2

반응 노트

불러오는 중…