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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169778Generated: November 1, 2026

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

https://huagongshe.com/reaction/2169778

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 numberUS09049862B2
Source datasetuspto-grants-2015_06
ORD IDord-37a3078c66304d2ca09233e3f1395e77
Source noteuspto-grants-2015_06