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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086708Generated: October 23, 2026

Hydrochloric Acid → 4-Acetyl-2-fluorobenzene-1-sulfonamide

https://huagongshe.com/en/reaction/2086708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
ReactantSodium NitrateHCID 24268—
Reactant1-(4-Amino-3-fluorophenyl)ethan-1-oneHCID 3018463—
CatalystCupric chloride dihydrateHCID 61482—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product4-Acetyl-2-fluorobenzene-1-sulfonamideHCID 2231696446.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-acetyl-2-fluoroaniline (5.0 g, 32.6 mmol, Krueger, G et al., Arzneim Forsch, 34, 11a, 1612 (1984)) in conc-HCl (24.0 mL), sodium nitrate (2.9 g, 42.4 mmol) in water (10 mL) was added at 0° C. After stirring for 1 h, the resultant yellow solution was added slowly to the suspension of copper (II) chloride dihydrate (1.7 g, 9.8 mmol) and sulfur dioxide (10 g, 156 mmol) in acetic acid (25 mL) at 0° C. The mixture was stirred for 30 min at 0° C. and poured into ice water (200 mL) and extracted with CH2Cl2 (80 mL×2). The extracts was cooled to 0° C. and 25% aqueous ammonia (70 mL) was added slowly and stirred for 1 h at room temperature. The mixture was concentrated and the residual solid was suspended with ether and collectted by filteration to give the title compound (3.3 g, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727238B2
Source datasetuspto-grants-2004_04
ORD IDord-38ef4584ee1c4d61886c70f6a6caef11
Source noteuspto-grants-2004_04