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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746746Generated: October 30, 2026

Tetrahydrofuran → HCID 24893993, compound

https://huagongshe.com/reaction/746746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriphosgeneHCID 94429—
Reactant4-Amino-N-(2-benzoylphenyl)benzene-1-sulfonamideHCID 69308994—
SolventTriethylamineHCID 8471—
ProductHCID 24893993HCID 24893993—

Reaction Conditions

Temperature0 °C

Reaction Steps

Triphosgene (28 mg, 1/3 equiv) was dissolved in 1 mL of THF and the solution cooled to 0° C. A solution of 4-amino-N-(2-benzoylphenyl)benzenesulfonamide (100 mg) in 3 mL of THF and 0.15 mL of triethylamine was added therto, and the reaction mixture was warmed to rt and stirred for 30 minutes. A solution of tetrahyhdrofurfuryl alcohol (44 mg, 1.5 equiv) in 3 mL of THF and 0.15 mL of triethylamine was added thereto and the reaction mixture was left stirring overnight. The reaction was quenched with water and diluted with EtOAc. The organic layer was washed once each with water and brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The title product was obtained following flash chromatography (10% to 95% EtOAc/hexanes). ESMS, M+H+ found: 481.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393873B2
Source datasetuspto-grants-2008_07
ORD IDord-d0db8c8263cb43b486ab5a2f1e9e67ce
Source noteuspto-grants-2008_07