HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746746Generated: October 30, 2026
Tetrahydrofuran → HCID 24893993, compound
https://huagongshe.com/reaction/746746
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | 4-Amino-N-(2-benzoylphenyl)benzene-1-sulfonamide | HCID 69308994 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 24893993 | HCID 24893993 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07393873B2 |
|---|
| Source dataset | uspto-grants-2008_07 |
|---|
| ORD ID | ord-d0db8c8263cb43b486ab5a2f1e9e67ce |
|---|
| Source note | uspto-grants-2008_07 |
|---|