Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789574Generated: October 30, 2026

Sulfur Dioxide → Lithium 3-chloro-4-ethoxycarbonyl-1-methylpyrazole-5-sulfinate

https://huagongshe.com/reaction/1789574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfur DioxideHCID 1119—
ReactantLithium diisopropylamideHCID 2724682—
ReactantEthyl 3-chloro-1-methyl-1H-pyrazole-4-carboxylateHCID 13687029—
SolventDiethyl EtherHCID 3283—
ProductLithium 3-chloro-4-ethoxycarbonyl-1-methylpyrazole-5-sulfinateHCID 23704643—

Reaction Conditions

Temperature-60 °C

Reaction Steps

5.0 g of ethyl 3-chloro-1-methylpyrazole-4-carboxylate was dispersed in dry diethyl ether under cooling at -60° C. or lower. Into this solution there was added lithium diisopropylamide (1.2 molar equivalent) and after stirring for an hour sulfur dioxide gas was passed into this solution for 30 minutes. After stirring at -60° C. for 2 hours the reaction mixture was stirred at room temperature for 2 hours. Filtration and drying of the precipitate gave 6.0 g of lithium 3-chloro-4-ethoxycarbonyl-1-methylpyrazole-5-sulfinate. This product was added into a solution of 100 ml of ice-water and 100 ml of dichloromethane and 6.0 g of N-chloro succinimide was added thereinto at 0°-5° C. After stirring for 45 minutes at room temperature the dichloromethane layer was separated and water layer was extracted with 100 ml of dichloromethane. The combined dichloromethane solution of 3-chloro-4-ethoxycarbonyl-1-methylpyrazole-5-sulfonyl chloride (b.p.: 133° C./ 0.25 mmHg.) was added dropwise into 80 ml of aqueous ammonia (28%) under cooling at 10° C. After stirring for an hour, evaporation of the solvent gave 3.6 g of 3-chloro-4-ethoxycarbonyl-1-methylpyrazole-5-sulfonamide. m.p.: 121°-123° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04689417
Source datasetuspto-grants-1987_08
ORD IDord-e765de5f47654addb30791e3c03fffd2
Source noteuspto-grants-1987_08