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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041966Generated: October 31, 2026

4-(1,3-Oxazol-5-yl)benzenesulphonyl chloride → HCID 59577086, compound

https://huagongshe.com/reaction/2041966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1,3-Oxazol-5-yl)benzenesulphonyl chlorideHCID 2776415—
ReactantAzane;hydrateHCID 12896473—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59577086HCID 5957708687%

Reaction Steps

To a stirred solution of 4-(1,3-oxazol-5-yl)benzenesulfonyl chloride (1.00 g, 4.10 mmol) in tetrahydrofuran (15.0 mL) was added 25% ammonia water solution (5.00 mL) at room temperature. After 1 h the reaction mixture was partitioned between ethyl acetate (100.0 mL) and 1.0 N hydrochloric acid (10.0 mL) and separated. The organic layer was washed with water (2×40 mL), saturated sodium chloride (80 mL), dried (MgSO4), filtered. The filtrate was concentrated under reduced pressure to provide 4-(1,3-oxazol-5-yl)benzenesulfonamide (800 mg, 87%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586571B2
Source datasetuspto-grants-2013_11
ORD IDord-a28aad63a6414442bf5b67ddc5d3a7d7
Source noteuspto-grants-2013_11