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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216225Generated: November 1, 2026

Hydrochloric Acid → 3-Bromo-4-fluorobenzene-1-sulfonyl chloride

https://huagongshe.com/reaction/2216225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
ReactantNitric acid, 1,1-dimethylethyl esterHCID 164756—
Reactant3-Bromo-4-fluoroanilineHCID 2779286—
CatalystCupric ChlorideHCID 24014—
SolventDichloromethane methanolHCID 21226129—
Product3-Bromo-4-fluorobenzene-1-sulfonyl chlorideHCID 2188673359%

Reaction Conditions

Temperature-5 °C

Reaction Steps

Concentrated HCl (1.93 mL, 23.16 mmol) was added to a solution of 3-bromo-4-fluoro-phenylamine ((Example 265: part a) 2.2 g, 11.58 mmol) in 18 mL of 2:1 DCM/MeOH. A precipitate appeared and another 9 mL of 2:1 DCM/MeOH was added. The solution was cooled to −5° C. and tert-butylnitrate (2.71 mL, 23.16 mmol) was added dropwise over 8 min. After stirring for 15 min, sulfur dioxide (˜5 mL) was condensed into the reaction, followed by addition of copper (II) chloride (592 mg, 3.47 mmol) (gas evolution). The solvent was removed in vacuo and the residue was purified by SiO2 flash column chromatography to yield the title compound (1.9 g, 59%). 1H-NMR (CDCl3): δ 8.31 (dd, 1H, J=2.3, 5.8 Hz), 8.04 (ddd, 1H, J=2.6, 4.1, 8.8 Hz), 7.39 (dd, 1H, J=7.7, 8.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109354B2
Source datasetuspto-grants-2006_09
ORD IDord-ed4da9165836405aa8b153108852e1b1
Source noteuspto-grants-2006_09