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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227581Generated: October 25, 2026

Hexachloroethane → 3-Chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamide

https://huagongshe.com/reaction/227581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexachloroethaneHCID 6214—
ReactantN,N-dimethyl-1H-pyrazole-1-sulfonamideHCID 10954038—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3-Chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamideHCID 21113388—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of N-dimethylsulfamoylpyrazole (188.0 g, 1.07 mol) in dry tetrahydrofuran (1500 mL) at −78° C. was added dropwise a solution of 2.5 M n-butyl-lithium (472 mL, 1.18 mol) in hexane while maintaining the temperature below −65° C. Upon completion of the addition the reaction mixture was maintained at −78° C. for an additional 45 minutes, after which time a solution of hexachloroethane (279 g, 1.18 mol) in tetrahydrofuran (120 mL) was added dropwise. The reaction mixture was maintained for an hour at −78° C., warmed to −20° C. and then quenched with water (1 L). The reaction mixture was extracted with methylene chloride (4×500 mL); the organic extracts were dried over magnesium sulfate and concentrated. The crude product was further purified by chromatography on silica gel using methylene chloride as eluent to afford the title product compound as a yellow oil (160 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560564B2
Source datasetuspto-grants-2009_07
ORD IDord-9657c2a711e3481a9f253b225c851a9f
Source noteuspto-grants-2009_07