HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654019Generated: October 25, 2026
Triethylamine → 3-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzenesulfonic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-N-methylethylamide]
https://huagongshe.com/reaction/654019
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzenesulfonic acid chloride | HCID 15057617 | — |
| Reactant | 1-(2,2-Dimethyl-1,3-dioxolan-4-yl)-2-(methylamino)ethan-1-ol | HCID 15057653 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[N-(4-Fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzenesulfonic acid-[2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-N-methylethylamide] | HCID 67899878 | — |
Reaction Steps
8.36 g (20 mmol) of 3-[N-(4-fluoro-2-trifluoromethylphenyl)sulfamoyl]-benzenesulfonic acid chloride is dissolved in 40 ml of tetrahydrofuran, 2.52 g (25 mmol) of triethylamine and 4.03 (25 mmol) of 2-hydroxy-2-(2,2-dimethyl-1,3-dioxolan-4-yl)-N-methylethylamine are added and stirred for 3 hours at 45° C. The reaction mixture is then concentrated by evaporation under reduced pressure, the residue is extracted with ethyl acetate and the extract is chromatographed on silica gel 60 (Merck) with ethyl acetate/hexane. 9.35 g (16.8 mmol)=84% of the theoretical yield is obtained as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05130119 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-a76d1f7cf3dc40a2aff7c1ef54e73eb8 |
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| Source note | uspto-grants-1992_07 |
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