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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181870Generated: October 25, 2026

Chlorosulfonic acid → BUTTPARK 120\07-29

https://huagongshe.com/reaction/2181870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
Reactant1-Methoxy-2-(trifluoromethyl)benzeneHCID 2775251—
SolventChloroformHCID 6212—
ProductBUTTPARK 120\07-29HCID 2248238456.2%

Reaction Steps

A solution of 1-methoxy-2-(trifluoromethyl)benzene (10.0 g, 56.8 mmol) in dry chloroform (76 mL) was cooled to 0° C. and treated with chlorosulfonic acid (7.55 mL, 113.5 mmol) drop-wise under argon. After the addition was completed, the reaction mixture was gradually warmed to room temperature and stirred overnight. The reaction was quenched by pouring the mixture slowly onto ice. The separated, aqueous phase was extracted with chloroform (3×). The combined organic phase was washed sequentially with a saturated, aqueous sodium chloride solution (2×) and water. The organic phase was dried over anhydrous magnesium sulfate and concentrated in vacuo to yield the title compound (8.77 g. 31.9 mmol, 56%) as a gray solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894061B2
Source datasetuspto-grants-2005_05
ORD IDord-454d07b0abb14def93e86a2a0fecf95b
Source noteuspto-grants-2005_05