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2-Chloro-1-cyclohexyl-4-(1,2,2-trichloroethyl)benzene → 3-chloro-4-cyclohexyl-1-ethynylbenzene

HRID 1606279
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반응식

HRID 1606279 반응식
Cl[CH:2](Cl)[CH:3]([C:5]1[CH:10]=[CH:9][C:8]([CH:11]2[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]2)=[C:7]([Cl:17])[CH:6]=1)Cl.C[Li]>CCOCC>[Cl:17][C:7]1[CH:6]=[C:5]([C:3]#[CH:2])[CH:10]=[CH:9][C:8]=1[CH:11]1[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 214442512-Chloro-1-cyclohexyl-4-(1,2,2-trichloroethyl)benzeneHCID 178418348HCID 178418348, 화합물

생성물 1

HCID 101768033-chloro-4-cyclohexyl-1-ethynylbenzene

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

β.β,α,3-tetrachloro-4-cyclohexylphenylethane (55.8 g.; 0.17 moles) is dissolved in anhydrous ether (100 ml). The solution is cooled in an ice-bath with stirring under nitrogen. Methyl lithium (2.3 M in ether; 300 cc) is added dropwise and the mixture stirred in the icebath for 2.5 hours before destroying the excess methyl lithium with ice. The ethereal fraction is washed thoroughly with saline until the washings are neutral. Removal of solvent gives 3-chloro-4-cyclohexyl-1-ethynylbenzene (b.p. 82°-88°/0.15 m).

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후처리

  1. temperatureThe solution is cooled in an ice-bath
  2. stirringthe mixture stirred in the icebath for 2.5 hours
  3. custombefore destroying the excess methyl lithium with ice
  4. washThe ethereal fraction is washed thoroughly with saline until the washings
  5. customRemoval of solvent

출처 및 근거

ORD 기록
ord-aa4a3cfffc2d4207a287e4bd77d121fa
출처 데이터셋
uspto-grants-1976_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03952067

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