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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518758Generated: October 26, 2026

Thionyl Chloride → 3-(N-allylsulfamoyl)benzoyl isothiocyanate

https://huagongshe.com/reaction/518758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-((Prop-2-en-1-yl)sulfamoyl)benzoic acidHCID 257468—
ReactantIsothiocyanatopotassiumHCID 10931372—
Solvent1,2-DichloroethaneHCID 11—
Product3-(N-allylsulfamoyl)benzoyl isothiocyanateHCID 8669282830.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 3-(N-allylsulfamoyl)benzoic acid (2 g, 8.29 mmol) in 1,2-dichloroethane (25 mL) was added thionyl chloride (1.271 mL, 17.41 mmol) dropwise. The suspension was stirred for 2 hours at 80° C. After 2 hours, the reaction mixture was concentrated to an off-white solid. The solid was redissolved in 25 mL acetone, and potassium isothiocyanate (0.967 g, 9.95 mmol) was added. A precipitate formed immediately upon addition. The reaction was stirred at 50° C. After 2 hours, the reaction was filtered, concentrated, and adsorbed onto a silca-gel pre column. The residue was purified by column chromatography, eluting with 20-100% EtOAc in hexanes, to provide 3-(N-allylsulfamoyl)benzoyl isothiocyanate as an off-white solid (0.71 g, 30.3% yield). MS, m/z (C11H10N2O3S2): calcd, 282.0. found, 282.9 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115127B2
Source datasetuspto-grants-2015_08
ORD IDord-41dbcc4d7ae84c169c6f90dfa17d4961
Source noteuspto-grants-2015_08