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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352412Generated: November 2, 2026

Sulfuryl chloride → 4-n-Butoxy-3-chloro-1,1,1-trifluorobut-3-en-2-one

https://huagongshe.com/reaction/2352412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
ReactantButoxyvinyl trifluoromethyl ketoneHCID 2782641—
SolventDichloromethaneHCID 6344—
Product4-n-Butoxy-3-chloro-1,1,1-trifluorobut-3-en-2-oneHCID 5444845492.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

28.0 g (0.22 mole) of sulphuryl chloride in 60 ml of dichloromethane are added dropwise with stirring to 39.0 g (0.2 mole) of 4-n-butoxy-1,1,1-trifluoro-but-3-en-2-one in 200 ml of dichloromethane at 0° C. After stirring for 4 hours at 0° C., the solvent and unreacted sulphuryl chloride are distilled off and the residue is distilled slowly under reduced pressure. 42.5 g of pale yellow 4-n-butoxy-3-chloro-1,1,1-trifluorobut-3-en-2-one of boiling point 105°-106° C./12 mbar, nD20 =1.4484 are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04876393
Source datasetuspto-grants-1989_10
ORD IDord-0192ec466e904ec8b0dafeb7a17b6637
Source noteuspto-grants-1989_10