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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885053Generated: November 1, 2026

Dimethylformamide → HCID 23505221, compound

https://huagongshe.com/reaction/1885053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantHCID 15906661HCID 15906661—
Reactant2,2,3,3-Tetrafluoropropyl nonafluorobutane-1-sulfonateHCID 23505222—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
ProductHCID 23505221HCID 23505221—

Reaction Conditions

Temperature120 °C

Reaction Steps

1.200 g (4.3 mmol) of potassium tert-butoxide and 1.917 g (4.3 mmol) of 2,2,3,3-tetrafluoropropyl perfluorobutanesulfonate were introduced into 30 ml of DMF in a vessel. At RT, 1200 g (4.3 mol) of methyl 2-chloro-3-hydroxy-4-ethylsulfonylbenzoate were added and the mixture was then heated at 120° C. for 7 h. It was subsequently introduced into water and subjected to extraction with diisopropyl ether. The combined organic phases were washed with water, dried over Na2SO4, and concentrated. Drying under an oil pump vacuum gave methyl 2-chloro-3-(2,2,3,3-tetrafluoropropyloxy)-4-ethylsulfonylbenzoate as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06768025B2
Source datasetuspto-grants-2004_07
ORD IDord-21ca817eed6343f593b0fa19883730cc
Source noteuspto-grants-2004_07