Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442976Generated: October 29, 2026

3-Cyanobenzene-1-sulfonyl chloride → HCID 54212462, compound

https://huagongshe.com/reaction/442976

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyanobenzene-1-sulfonyl chlorideHCID 2801360—
ReactantResorcinol, 5-methyl-, monohydrateHCID 3083941—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventSodium BicarbonateHCID 516892—
ProductHCID 54212462HCID 5421246283%

Reaction Steps

Orcinol monohydrate (1.42 g, 10.0 mmol) and 3-cyanobenzenesulfonyl chloride (2.02 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 oil (2.40 g, 83%). 1H-NMR (300 MHz, CDCl3) δ 8.12 (s, 1H), 8.07 (d, J=8.0 Hz, 1H), 7.93 (d, J=7.8 Hz, 1H), 7.68 (t, J=7.9 Hz, 1H), 6.56 (s, 1H), 6.36 (s, 1H), 6.30 (s, 1H), 5.35 (s, 1H), 2.22 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891909
Source datasetuspto-grants-1999_04
ORD IDord-d3e2707b77eb4087807400f39ec42584
Source noteuspto-grants-1999_04