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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731246Generated: November 1, 2026

Trifluoromethanesulfonic acid → HCID 54074415, compound

https://huagongshe.com/reaction/1731246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantHCID 53901951HCID 53901951—
SolventWaterHCID 962—
ProductHCID 54074415HCID 5407441552.5%

Reaction Steps

A portion (0.74 g) of the N-tert-butyl-3-(2-chloro-1,2-difluoroethenyl)-5-trimethylsilyl-2-thiophenesulfonamide prepared in (1) was treated with 4 ml of trifluoromethanesulfonic acid under stirring at room temperature for 2 hours. After completion of the reaction, the resulting product was poured into water and extracted with methylene chloride. The extracted layer was washed with water and dried. After distilling off methylene chloride under vacuum, the residual crystals were washed with a small amount of toluene and dried to obtain 0.26 g of 3-(2-chloro-1,2-difluoroethenyl)-2-thiophenesulfonamide having a melting point of 112° to 116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04620868
Source datasetuspto-grants-1986_11
ORD IDord-570e334749554b399440e9f0daf5e354
Source noteuspto-grants-1986_11