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Thionyl Chloride → 1-Benzyl-2-(chloromethyl)pyrrolidine

HRID 1253497
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HRID 1253497 반응식
[CH2:1]([N:8]1[CH2:12][CH2:11][CH2:10][CH:9]1[CH2:13]O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(Cl)([Cl:17])=O>C(Cl)(Cl)Cl>[CH2:1]([N:8]1[CH2:12][CH2:11][CH2:10][CH:9]1[CH2:13][Cl:17])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 562951(1-Benzylpyrrolidin-2-yl)methanol

생성물 1

HCID 30426421-Benzyl-2-(chloromethyl)pyrrolidine

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

Into a 5,000 ml 3-necked roundbottom flask, was placed a solution of (1-benzylpyrrolidin-2-yl)methanol (250. g, 1.30 mol) in chloroform (2,500 ml). This was followed by the dropwise addition of a solution of thionyl chloride (232. g, 1.95 mol) in chloroform (500 ml), while maintaining the internal temperature at room temperature (60 minute addition time). The resulting solution was heated to reflux for 2 hours. After cooling to ambient temperature, the mixture was concentrated, and the resulting residue was dissolved in 3,000 ml of ethyl acetate. Adjustment of the pH to 7 was accomplished by the addition of triethylamine. The resulting mixture was filtered and the filtrate was concentrated and the residue was purified by flash column chromatography (ethylacetate/petroleum ether gradient) to afford 1-benzyl-2-(chloromethyl)pyrrolidine.

후처리

  1. customInto a 5,000 ml 3-necked roundbottom flask, was placed
  2. addition(60 minute addition time)
  3. temperatureThe resulting solution was heated
  4. temperatureto reflux for 2 hours
  5. temperatureAfter cooling to ambient temperature
  6. concentrationthe mixture was concentrated
  7. dissolutionthe resulting residue was dissolved in 3,000 ml of ethyl acetate
  8. additionAdjustment of the pH to 7 was accomplished by the addition of triethylamine
  9. filtrationThe resulting mixture was filtered
  10. concentrationthe filtrate was concentrated
  11. customthe residue was purified by flash column chromatography (ethylacetate/petroleum ether gradient)

출처 및 근거

ORD 기록
ord-d21cc5e537544f998cf5b95260a136fc
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08455477B2

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