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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442921Generated: October 30, 2026

2,1,3-Benzothiadiazole, 4-chlorosulfonyl- → HCID 54444075, compound

https://huagongshe.com/reaction/442921

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,1,3-Benzothiadiazole, 4-chlorosulfonyl-HCID 2735459—
ReactantResorcinol, 5-methyl-, monohydrateHCID 3083941—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventSodium BicarbonateHCID 516892—
ProductHCID 54444075HCID 5444407579.1%

Reaction Steps

Orcinol monohydrate (1.42 g, 10.0 mmol) and benzo-2,1,3-thiadiazole-4-sulfonyl chloride (2.35 g, 10.0 mmol) were mixed in saturated aqueous NaHCO3 (30 mL) and diethyl ether (30 mL). The biphasic mixture was stirred vigorously at ambient temperature overnight. The reaction mixture was diluted with water (50 mL) and extracted into ethyl acetate (3×50 mL). The organic phase was washed with brine (2×50 mL) and dried over Na2SO4. After removing the solvent in vacuo, the residue was purified by flash column chromatography (dichloromethane to 5% ethyl acetate in dichloromethane) to give the title compound as a pale yellow solid (2.55 g, 79%). 1H-NMR (300 MHz, CDCl3) δ 8.34 (d, J=8.8 Hz, 1H), 8.26 (d, J=7.1 Hz, 1H), 7.72 (t, J=8.8 Hz, 1H), 6.53 (s, 1H), 6.47 (s, 1H), 6.37 (s, 1H), 5.24 (s, 1H), 2.19 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891909
Source datasetuspto-grants-1999_04
ORD IDord-6338318763814c3f808a1db19d3720ff
Source noteuspto-grants-1999_04