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Thionyl Chloride → 10-Chloro-1-decene

HRID 1199866
ノート
印刷プレビュー

反応式

HRID 1199866 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 24386Thionyl ChlorideHCID 256129-Decen-1-ol

生成物 1

HCID 1174513910-Chloro-1-decene収率 95.3%

試薬・触媒・溶媒 2

HCID 1049Pyridine触媒HCID 6344Dichloromethane溶媒

実験手順

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%)

後処理

  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

出典と根拠

ORDレコード
ord-f1bc5469004c4bc2ac4b6826801d7aaa
出典データセット
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04904065

反応ノート

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