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Dibromomethane → 1-(4-Chlorophenyl)-2-cyclopropylpropan-1-ol

HRID 964733
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HRID 964733 반응식
[CH3:1][CH:2]([CH:5]([C:7]1[CH:12]=[CH:11][C:10]([Cl:13])=[CH:9][CH:8]=1)[OH:6])[CH:3]=[CH2:4].Br[CH2:15]Br>CCOCC.[Zn].[Cu]Cl>[Cl:13][C:10]1[CH:11]=[CH:12][C:7]([CH:5]([OH:6])[CH:2]([CH:3]2[CH2:15][CH2:4]2)[CH3:1])=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 3024DibromomethaneHCID 113676051-(4-Chloro-phenyl)-2-methyl-but-3-en-1-ol

생성물 1

HCID 190783851-(4-Chlorophenyl)-2-cyclopropylpropan-1-ol수율 73%

시약·촉매·용매 3

HCID 23994Zinc촉매HCID 62652Cuprous chloride촉매HCID 3283Diethyl Ether용매

실험 절차

3-Methyl-4-(4-chlorophenyl)but-1-en-4-ol (63.68 g, approximately 90% pure, approximately 292 mmol), dibromomethane (45.5 ml, 648 mmol), zinc dust (84.75 g, 1.296 mol) and copper(I) chloride (12.83 g, 130 mmol) in dry ether (180 ml) were heated under reflux in a sonic bath for 31/2 hours. The mixture was then filtered (celite) and the filtrate poured into 2M hydrochloric acid. The mixture was extracted with ether and the combined extracts washed with water, saturated aqueous sodium bicarbonate solution and water, dried and evaporated in vacuo. Chromatography [SiO2, hexane-ethyl acetate (100:0) to (80:20)] gave 1-(4-chlorophenyl)-2-cyclopropylpropan-1-ol (44.72 g, 73%).

후처리

  1. temperatureunder reflux in a sonic bath for 31/2 hours
  2. filtrationThe mixture was then filtered (celite)
  3. additionthe filtrate poured into 2M hydrochloric acid
  4. extractionThe mixture was extracted with ether
  5. washthe combined extracts washed with water, saturated aqueous sodium bicarbonate solution and water
  6. customdried
  7. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-a42d0a4547104423aafb481909f9e24c
출처 데이터셋
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05770741

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