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Thionyl Chloride → 10-Chloro-1-decene

HRID 2352586
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HRID 2352586 반응식
[CH2:1](O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH:9]=[CH2:10].S(Cl)([Cl:14])=O>N1C=CC=CC=1.ClCCl>[Cl:14][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH:9]=[CH2:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24386Thionyl Chloride2회HCID 256129-Decen-1-ol

생성물 1

HCID 1174513910-Chloro-1-decene수율 95.3%

시약·촉매·용매 2

HCID 1049Pyridine촉매HCID 6344Dichloromethane용매

실험 절차

10 drops of pyridine was added to 26.0 g of 9-decene-1-ol and the mixture was placed in an eggplant type flask. Into the flask was then dropped 24.0 g of thionyl chloride while cooling with ice. After dropping thionyl chloride, reaction was carried out for 8.5 hours at 70° C. After the reaction, the resulting reaction solution was diluted with dichloromethane and was washed with an aqueous potassium hydroxide solution. The organic phase was dried over magnesium sulfate and was then concentrated under reduced pressure. The resulting residue was purified by column chromatography to obtain 27.7 g of 10-chloro-1-decene. (Yield: 95%).

후처리

  1. customthe mixture was placed in an eggplant type flask
  2. temperaturewhile cooling with ice
  3. customAfter the reaction
  4. customthe resulting reaction solution
  5. washwas washed with an aqueous potassium hydroxide solution
  6. dry with materialThe organic phase was dried over magnesium sulfate
  7. concentrationwas then concentrated under reduced pressure
  8. customThe resulting residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-756996190d1a437cae52fdab262cc154
출처 데이터셋
uspto-grants-1989_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04877858

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