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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277572Generated: October 30, 2026

4-Fluoro-3-(morpholine-4-sulfonyl)benzoic acid → 4-Mercapto-3-(morpholine-4-sulfonyl)-benzoic Acid

https://huagongshe.com/reaction/277572

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluoro-3-(morpholine-4-sulfonyl)benzoic acidHCID 692716—
ReactantSodium hydrosulfide hydrateHCID 16211346—
SolventDimethylformamideHCID 6228—
Product4-Mercapto-3-(morpholine-4-sulfonyl)-benzoic AcidHCID 2262903989.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium hydrosulfide monohydrate (237 mg, 4.3 mmol) was added to a solution of 4-fluoro-3-(morpholine-4-sulfonyl)-benzoic acid (Example 6, 350 mg, 1.2 mmol) in DMF (15 mL) and the reaction mixture was heated at 60° C. for 20 hours under N2. After cooling to room temperature and quenching with 2M HCl, the reaction mixture was partitioned between ethyl acetate and water. Further extraction of the aqueous layer with ethyl acetate, combination of all organic layers, drying and concentration provided a white powder (326 mg, 89% yield): 1HNMR DMSO-d6) δ2.99 (t, J=4 Hz, 4H), 3.58 (t, J=4. Hz, H), 7.48 (d, J=8 Hz,1H), 7.87 (dd, J=8, 2 Hz, 1H), 8.29 (d, J=2 Hz, 1H), 13.20 (s, 1H): MS (ESI) [M−H]− m/z 304.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355633B1
Source datasetuspto-grants-2002_03
ORD IDord-e294ca167e124d8e8f95b243a2f7dcb4
Source noteuspto-grants-2002_03