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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-((Prop-2-en-1-yl)sulfamoyl)benzoic acid | HCID 257468 | — |
| Reactant | Isothiocyanatopotassium | HCID 10931372 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 3-(N-allylsulfamoyl)benzoyl isothiocyanate | HCID 86692828 | 30.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115127B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-41dbcc4d7ae84c169c6f90dfa17d4961 |
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| Source note | uspto-grants-2015_08 |
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