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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Thionyl Chloride → 10-Chloro-1-decene

HRID 1199866
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반응식

HRID 1199866 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 ChlorideHCID 256129-Decen-1-ol

생성물 1

HCID 1174513910-Chloro-1-decene수율 95.3%

시약·촉매·용매 2

HCID 1049Pyridine촉매HCID 6344Dichloromethane용매

실험 절차

To 26.0 g of 9-decene-1-ol was added 10-drops of pyridine and the mixture was placed into an eggplant flask. To the eggplant flask was added dropwise 24.0 g of thionyl chloride during cooling with ice. After dropping, the mixture was reacted for 8.5 hours at 70° C. After the conclusion of the reaction, the reaction product was diluted with dichloromethane and then washed with an aqueous potassium carbonate solution. The reaction solution was then dried over magnesium sulfate and subsequently 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 into an eggplant flask
  2. temperatureduring cooling with ice
  3. customthe mixture was reacted for 8.5 hours at 70° C
  4. customAfter the conclusion of the reaction
  5. washwashed with an aqueous potassium carbonate solution
  6. dry with materialThe reaction solution was then dried over magnesium sulfate
  7. concentrationsubsequently concentrated under reduced pressure
  8. customThe resulting residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-f1bc5469004c4bc2ac4b6826801d7aaa
출처 데이터셋
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04904065

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