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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442924Generated: October 31, 2026

3-Methylbenzenesulphonyl chloride → HCID 10934765, compound

https://huagongshe.com/reaction/442924

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methylbenzenesulphonyl chlorideHCID 2734595—
ReactantResorcinol, 5-methyl-, monohydrateHCID 3083941—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventSodium BicarbonateHCID 516892—
ProductHCID 10934765HCID 1093476594.3%

Reaction Steps

Orcinol monohydrate (1.42 g, 10.0 mmol) and 3-methylbenzenesulfonyl chloride (1.60 g, 8.0 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 (3×40 mL). The organic phase was washed with brine (2×30 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 yellow oil (2.1 g, 76%). 1H-NMR (300 MHz, CDCl3) δ 7.68 (s, 1H), 7.64 (d, J=7.9 Hz, 1H), 7.45 (t, J=7.8 Hz, 1H), 7.40 (t, J=7.6 Hz, 1H), 6.54 (s, 1H), 6.39 (s, 1H), 6.32 (s, 1H), 5.33 (s, 1H), 2.41 (s, 3H), 2.21 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891909
Source datasetuspto-grants-1999_04
ORD IDord-71004d10adc34bdd82d652e390f27bb6
Source noteuspto-grants-1999_04