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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990600Generated: October 31, 2026

Hydrochloric Acid → 2-Fluoro-5-oxiranyl-benzenesulfonamide

https://huagongshe.com/reaction/990600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
Reactant5-(2-Bromoacetyl)-2-fluorobenzenesulphonamideHCID 11808590—
SolventMethanolHCID 887—
Product2-Fluoro-5-oxiranyl-benzenesulfonamideHCID 1098771248.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 0.5 g (1.7 mmol) of 5-bromoacetyl-2-fluoro-benzenesulfonamide V in 20 mL MeOH was cooled to 0° C. NaBH4 26 mg (0.67 mmol) was added and the reaction was stirred at 0° C. for 15 min. 4 mL of 1N NaOH was added and the reaction was stirred at 0° C. for 4 hrs. The reaction was adjusted to pH 6 by addition of dilute HCl. The volatiles were evaporated and the residue dissolved in EtOAc, washed with H2O, dried over Na2SO4 and evaporated. The product was purified by column chromatography on silica gel eluting with CH2Cl2/MeOH::9/1 to give 180 mg of VI (48%); mp 100-103° C.TLC:CH2Cl2/MeOH::9/1 single-spot material Rƒ 0.65.1H-NMR (300 MHz DMSO-D6) δ: (2.82, m, 1H), (3.14, m, 1H), (4.06, m, 1H), (7.40, t, 1H), (7.56, m, 1H), (7.66, m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06461822B2
Source datasetuspto-grants-2002_10
ORD IDord-7d630e878c6b4ee3b761c84695749569
Source noteuspto-grants-2002_10