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Thionyl Chloride → (1-Chloroethyl)-2,4-hexadienoate

HRID 35275
ノート
印刷プレビュー

反応式

HRID 35275 の反応式
[C:1]([OH:8])(=[O:7])/[CH:2]=[CH:3]/[CH:4]=[CH:5]/[CH3:6].S(Cl)([Cl:11])=O.CC1OC(C)O[CH:16]([CH3:21])O1>[Cl-].[Zn+2].[Cl-]>[Cl:11][CH:16]([O:7][C:1](=[O:8])[CH:2]=[CH:3][CH:4]=[CH:5][CH3:6])[CH3:21]
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 3

HCID 24386Thionyl ChlorideHCID 31264ParaldehydeHCID 643460Sorbic Acid2 回

生成物 1

HCID 53809045(1-Chloroethyl)-2,4-hexadienoate収率 64.2%

試薬・触媒・溶媒 1

HCID 3007855Zincchloride触媒

実験手順

A mixture of 5.6 g. (50 mmoles) of sorbic acid and 7.8 g. (65 mmoles) of thionyl chloride was stirred at a room temperature for one hour, and then reacted at 50° C. for 30 minutes with stirring to complete the reaction. The end point of the reaction was judged by cessation of SO2 gas production and disappearance (dissolution) of sorbic acid. The resulting reaction mixture was cooled with ice, and then 0.27 g. (2 mmoles) of 96% zinc chloride was added thereto. After adding dropwise 2.2 g. of paraldehyde at 0° C., the reaction was carried out at a room temperature for one hour. The resulting reaction mixture was treated and purified in the same manner as in Reference Example 1 to give 5.43 g. (yield: 64.2%) of the desired compound being a clear solution.

後処理

  1. additionA mixture of 5.6 g
  2. customreacted at 50° C. for 30 minutes
  3. customthe reaction
  4. customThe resulting reaction mixture
  5. temperaturewas cooled with ice
  6. additionAfter adding dropwise 2.2 g
  7. customThe resulting reaction mixture
  8. additionwas treated
  9. custompurified in the same manner as in Reference Example 1
  10. customto give 5.43 g

出典と根拠

ORDレコード
ord-8d3fb801a85840e4b1294e2a03ba2f4c
出典データセット
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04766148

反応ノート

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