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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467227Generated: October 30, 2026

Chlorosulfonyl isocyanate → HCID 19813655, compound

https://huagongshe.com/reaction/467227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
ReactantHCID 19813653HCID 19813653—
SolventEthyl AcetateHCID 8857—
ProductHCID 19813655HCID 1981365583.8%

Reaction Conditions

Temperature3 °C

Reaction Steps

At 3° C., 3.6 g (0.026 mole) of chlorosulfonyl isocyanate are added to a solution of 6.4 g (0.02 mole) of N-(4-methyl-6-trifluoromethyl-pyrimidin-2-yl)-2-trifluoromethylaniline in 100 ml of ethyl acetate. After stirring the batch for 2 hours at 3° C., 100 ml of ethyl acetate and 50 ml of ice-water are added. The aqueous phase is separated off, and the organic phase is washed with sodium chloride solution, dried with sodium sulfate and concentrated by evaporation in a rotary evaporator. The crystals remaining are triturated with hexane, filtered off and dried in vacuo at 40° C. 6.1 g (83.8%) of the title compound of formula ##STR11## are isolated in the form of crystals having a melting point of 150°-153° C. (Comp. No. 1.020).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05159078
Source datasetuspto-grants-1992_10
ORD IDord-c20054233f684d369c688c8e060c803b
Source noteuspto-grants-1992_10