Pyridine → 1-Cyclohexyl-4-chloromethyl-3,3-diphenyl-2-pyrrolidinone

HRID 2285775노트

반응식

HRID 2285775 반응식
[CH:1]1([N:7]2[CH2:11][CH:10]([CH2:12]O)[C:9]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[C:8]2=[O:26])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.S(Cl)([Cl:29])=O.N1C=CC=CC=1>C(Cl)(Cl)Cl>[Cl:29][CH2:12][CH:10]1[CH2:11][N:7]([CH:1]2[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]2)[C:8](=[O:26])[C:9]1([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

참가 물질

5

실험 절차

To 60.0 g. (0.17 mole) of 1-cyclohexyl-4-hydroxymethyl-3,3-diphenyl-2-pyrrolidinone in 400 ml. of chloroform was added 48.0 g. (0.40 mole) of thionylchloride with stirring. To this solution was added dropwise with ice bath cooling 40 g. (0.52 mole) of dry pyridine and the solution was refluxed for two hours. After concentrating in vacuo the residue was dissolved in chloroform and washed successively with dilute hydrochloric acid solution and dilute sodium hydroxide solution. The chloroform solution was dried (sodium sulfate), filtered, and concentrated in vacuo. The residue was recrystallized from isopropyl ether and after drying weighed 34.5 g. (55% yield) and melted at 124°-126° C.

후처리

  1. additionTo this solution was added dropwise with ice bath
  2. temperaturecooling 40 g
  3. concentrationAfter concentrating in vacuo the residue
  4. dissolutionwas dissolved in chloroform
  5. washwashed successively with dilute hydrochloric acid solution and dilute sodium hydroxide solution
  6. dry with materialThe chloroform solution was dried (sodium sulfate)
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe residue was recrystallized from isopropyl ether
  10. customafter drying

출처 및 근거

ORD 기록
ord-54aacdf3a5e44abc8f9da5944cd72f0c
출처 데이터셋
uspto-grants-1982_04
특허 번호
US04324791

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