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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39222Generated: October 23, 2026

Hydrochloric Acid → 2-Cyano-3-difluoromethoxyphenylsulfonyl chloride

https://huagongshe.com/en/reaction/39222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
ReactantSodium NitriteHCID 23668193—
Reactant2-Amino-6-difluoromethoxy-benzonitrileHCID 58100765—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-Cyano-3-difluoromethoxyphenylsulfonyl chlorideHCID 5810076791%

Reaction Conditions

Temperature5 °C

Reaction Steps

2-Amino-6-difluoromethoxy-benzonitrile (6.4 g, 35 mmol) is dissolved in glacial acetic acid (50 ml). Hydrochloric acid (37%, 12.7 g) is added dropwise at ambient temperature. This mixture is cooled to 5° C. and a solution of sodium nitrite (2.5 g, 36.4 mmol) in Water (8 ml) is added dropwise. The reaction mixture is stirred at 0° C. for 1 hour. The resulting diazonium salt solution is added dropwise at ambient temperature to a mixture of glacial acetic acid (100 ml) saturated at ambient temperature with sulfur dioxide and a solution of CuCl2 (2.18 g, 16.2 mmol) in water (5 ml). The resulting mixture is stirred at ambient temperature for 2 hours. The reaction mixture is poured into an ice/water and extracted three times with dichloromethane. The combined organic phases are dried over sodium sulfate and concentrated to give 2-Cyano-3-difluoromethoxy-benzenesulfonyl chloride (8.5 g, 91% yield) which is used without further purification. 1H-NMR (CDCl3, 400 MHz): 8.10 (d, 1H), 7.85 (t, 1H), 7.75 (d, 1H), 6.75 (t, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524896B2
Source datasetuspto-grants-2013_09
ORD IDord-8a94f41c9d4f4fdaa637af0309b079c2
Source noteuspto-grants-2013_09