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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442919Generated: October 26, 2026

2-(Trifluoromethoxy)benzene-1-sulfonyl chloride → HCID 53679268, compound

https://huagongshe.com/reaction/442919

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Trifluoromethoxy)benzene-1-sulfonyl chlorideHCID 2777215—
ReactantResorcinol, 5-methyl-, monohydrateHCID 3083941—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventSodium BicarbonateHCID 516892—
ProductHCID 53679268HCID 5367926857.4%

Reaction Steps

Orcinol monohydrate (1.42 g, 10.0 mmol) and 2-trifluoromethoxybenzenesulfonyl chloride (2.35 g, 9.0 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 yellow oil (1.80 g, 57%). 1H-NMR (300 MHz, CDCl3) δ 7.96 (d, J=7.9 Hz, 1H), 7.72 (t, J=7.8 Hz, 1H), 7.50 (d, J=8.1 Hz, 1H), 7.40 (t, J=7.8 Hz, 1H), 6.55 (s, 1H), 6.52 (s, 1H), 6.41 (s, 1H), 5.04 (s, 1H); 2.23 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891909
Source datasetuspto-grants-1999_04
ORD IDord-a710b30086ad405b9fee0e71f15f8324
Source noteuspto-grants-1999_04