Thionyl Chloride → HCID 14501734, compound
Reaction equation
[F:1][C:2]([F:10])([F:9])[CH2:3][O:4][CH2:5][C:6](O)=[O:7].S(Cl)([Cl:13])=O>C(Cl)(Cl)Cl>[F:1][C:2]([F:10])([F:9])[CH2:3][O:4][CH2:5][C:6]([Cl:13])=[O:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a 3-neck 500 ml round-bottom flask equipped with a magnetic stirrer, reflux condenser and addition funnel was added (2,2,2-trifluoroethoxy)acetic acid (30.90 g, 0.196 moles) and 250 ml of chloroform under nitrogen. Thionyl chloride (30.20 g, 0.250 moles) was added dropwise and the solution refluxed for 2 hours. The mixture was then concentrated by distillation of the chloroform and excess thionyl chloride. The remaining yellow oil was distilled in vacuo to give 18.9 g of the product as a colorless oil, bp 40°-48° C./20 mm.
Workup
- customTo a 3-neck 500 ml round-bottom flask equipped with a magnetic stirrer
- temperaturereflux
- additioncondenser and addition funnel
- temperaturethe solution refluxed for 2 hours
- concentrationThe mixture was then concentrated by distillation of the chloroform and excess thionyl chloride
- distillationThe remaining yellow oil was distilled in vacuo
Sources & evidence
- ORD record
- ord-40681304b10842c7b07f9c5deebeebed
- Source dataset
- uspto-grants-1989_07
- Patent number
- US04846873
Reaction notes
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