Propyltriphenylphosphonium bromide → 1-Carbobenzoxy-4-(1-butylidene)piperidine

HRID 223365

반응식

HRID 223365 반응식
[CH2:1]([Li])[CH2:2][CH2:3][CH3:4].[Br-].C([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)CC.[C:29]([N:39]1[CH2:44][CH2:43][C:42](=O)[CH2:41][CH2:40]1)([O:31][CH2:32][C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)=[O:30]>O1CCCC1>[C:29]([N:39]1[CH2:44][CH2:43][C:42](=[CH:1][CH2:2][CH2:3][CH3:4])[CH2:41][CH2:40]1)([O:31][CH2:32][C:33]1[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=1)=[O:30]

참가 물질

5

반응물 3

HCID 80374Propyltriphenylphosphonium bromideHCID 643496Benzyl 4-oxopiperidine-1-carboxylateHCID 178418339Butyllithium

생성물 1

HCID 205220201-Carbobenzoxy-4-(1-butylidene)piperidine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Butyl lithium (44 ml of 1.6 M in hexane) was added slowly to a stirred suspension of 27 g of (n-propyl)triphenylphosphonium bromide in 350 ml of tetrahydrofuran and the resulting solution was refluxed for 1 hour. The mixture was cooled in an ice bath and 18 g of N-carbobenzyloxy-4-piperidone was added. After stirring at room temperature of 0.5 hour, the solution was refluxed for 2 hours. The cooled mixture was concentrated under reduced pressure, partitioned between ether and water, and the ether layer was dried (sodium sulfate) and evaporated. The residue was filtered through silica gel with 20% ethyl acetate-hexane to give 10 g of 1-carbobenzoxy-4-(1-butylidene)piperidine as a colorless oil.

후처리

  1. temperaturethe resulting solution was refluxed for 1 hour
  2. temperatureThe mixture was cooled in an ice bath
  3. temperaturethe solution was refluxed for 2 hours
  4. concentrationThe cooled mixture was concentrated under reduced pressure
  5. custompartitioned between ether and water
  6. dry with materialthe ether layer was dried (sodium sulfate)
  7. customevaporated
  8. filtrationThe residue was filtered through silica gel with 20% ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-b3241550fb41428e92b1ccd841909194
출처 데이터셋
uspto-grants-1982_10
특허 번호
US04353900

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