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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692123Generated: October 30, 2026

Chlorosuccinimide → 2-(4-Tert-butyl-benzenesulfonylamino)-5-chloro-4-fluoro-benzoic acid

https://huagongshe.com/reaction/1692123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant2-(4-Tert-butyl-benzenesulfonylamino)-4-fluoro-benzoic acidHCID 45299887—
SolventAcetic AcidHCID 176—
Product2-(4-Tert-butyl-benzenesulfonylamino)-5-chloro-4-fluoro-benzoic acidHCID 5930303187.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-(4-tert-Butyl-benzenesulfonylamino)-4-fluoro-benzoic acid (23 g, 65.5 mmol) was added to 230 mL of stirring acetic acid in a 500 mL round bottom flask. N-chlorosuccinimide (17.5 g, 131 mmol) was then added and the mixture heated to 80° C. under a N2 atmosphere. The reaction was determined to be complete in seven hours according to LCMS analysis. The heat bath was subsequently removed and the reaction was quenched via the addition of 250 mL of a 50% solution of sodium metabisulfite. The mixture immediately formed a thick white slurry which was allowed to stir for approximately 15 minutes. Vacuum filtration of the slurry resulted in a white solid that was washed with a small amount of water and dried in vacuo to generate 22 g of 2-(4-tert-butyl-benzenesulfonylamino)-5-chloro-4-fluoro-benzoic acid (white solid, 87% yield): HPLC retention time=2.87 minutes; MS (ES) M+H expected 386.0, found 386.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153818B2
Source datasetuspto-grants-2012_04
ORD IDord-e15ff3a9e7c94f228df1e4b82e270e38
Source noteuspto-grants-2012_04