4-Methoxybiphenyl → HCID 22640158, 화합물

HRID 2415142노트

반응식

HRID 2415142 반응식
C([Li])CCC.[CH2:6]([N:13]1[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]1)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.CO[C:21]1[CH:26]=[CH:25][C:24]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)=[CH:23][CH:22]=1>CCCCCC.C1COCC1>[CH2:6]([N:13]1[CH2:18][CH2:17][N:16]([C:30]2[CH:31]=[CH:32][C:27]([C:24]3[CH:25]=[CH:26][CH:21]=[CH:22][CH:23]=3)=[CH:28][CH:29]=2)[CH2:15][CH2:14]1)[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1

참가 물질

6

반응물 3

HCID 119434-MethoxybiphenylHCID 759941-BenzylpiperazineHCID 178418339Butyllithium

생성물 1

HCID 22640158HCID 22640158, 화합물

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 8058Hexane용매

실험 절차

1.6 ml (0.05 mol) of butyllithium solution in n-hexane is added dropwise to a solution of 8.81 g (0.05 mol) of 1-benzylpiperazine in 50 ml of anhydrous THF under argon at 0° C. and stirred for one hour. Then 9.21 g (0.05 mol) of 4-methoxybiphenyl are added and the reaction mixture is refluxed for 12 hours. The solvent is then evaporated off, the residue is combined with 150 ml of 2 N hydrochloric acid followed by diethyl ether and the precipitate formed is filtered off. The precipitate is washed with diethyl ether, suspended in 20% sodium carbonate solution and extracted several times with dichloromethane. After drying over magnesium sulphate the solvent is removed and the residue is washed with ethyl acetate and diethyl ether.

후처리

  1. temperaturethe reaction mixture is refluxed for 12 hours
  2. customThe solvent is then evaporated off
  3. customthe precipitate formed
  4. filtrationis filtered off
  5. washThe precipitate is washed with diethyl ether
  6. extractionextracted several times with dichloromethane
  7. dry with materialAfter drying over magnesium sulphate the solvent
  8. customis removed
  9. washthe residue is washed with ethyl acetate and diethyl ether

출처 및 근거

ORD 기록
ord-6e64cfceef30490bafff1fdb7761382c
출처 데이터셋
uspto-grants-2004_11
특허 번호
US06818644B1

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