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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442936Generated: October 30, 2026

Benzenesulfonyl chloride, 2,5-dimethyl- → HCID 53837258, compound

https://huagongshe.com/reaction/442936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chloride, 2,5-dimethyl-HCID 87910—
ReactantResorcinol, 5-methyl-, monohydrateHCID 3083941—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventSodium BicarbonateHCID 516892—
ProductHCID 53837258HCID 5383725872%

Reaction Steps

Orcinol monohydrate (1.42 g, 10.0 mmol) and 2,5-dimethylbenzenesulfonyl chloride (2.05 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 2% ethyl acetate in dichloromethane) to give the title compound as a pale yellow oil (2.10 g, 72%). 1H-NMR (300 MHz, CDCl3) δ 7.65 (s, 1H), 7.29 (m, 1H), 7.25 (m, 1H), 6.50 (s, 1H), 6.38 (s, 1H), 6.30 (s, 1H), 5.27 (br s, 1H), 2.30 (s, 3H), 2.18 (s, 3H), 2.03 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891909
Source datasetuspto-grants-1999_04
ORD IDord-7dfbc2158a6e451b809d0d7f577b1b03
Source noteuspto-grants-1999_04