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

HRID 1614358

Reaction equation

HRID 1614358 reaction equation
[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]

Participants

5

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-7d06fcdc820e4f94b1c9d2cdb4ed5707
Source dataset
uspto-grants-1993_03
Patent number
US05196567

Linked notes

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