HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429804Generated: October 28, 2026
Water → 2-(2-Phenyl-ethen-1-yl)-3-difluoromethoxy-thiophene-2-carboxanilide
https://huagongshe.com/reaction/429804
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Aminostilbene | HCID 139378 | — |
| Reactant | 2-Thiophenecarbonyl chloride, 3-(difluoromethoxy)- | HCID 11127599 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(2-Phenyl-ethen-1-yl)-3-difluoromethoxy-thiophene-2-carboxanilide | HCID 69886413 | 189.2% |
Reaction Steps
At room temperature, a solution of 0.3 g (0.0015 mol) of 2-(2-phenyl-ethen-1-yl)-aniline in 2 ml of toluene is admixed with a solution of 0.15 g (0.0015 mol) of triethylamine in 10 ml of toluene. At room temperature, 0.33 g (0.0015 mol) of 3-difluoromethoxy-thiophene-2-carbonyl chloride are added to this mixture with stirring. The mixture is subsequently heated to 50° C. and stirred at this temperature for 2 hours. For work-up, the reaction mixture is then cooled to room temperature and admixed with water. The organic phase is separated off, dried over sodium sulphate and then concentrated under reduced pressure at 60° C. The residue that remains is chromatographed over silica gel using diethyl ether. Concentration of the eluate gives 0.53 g (95% of theory) of 2-(2-phenyl-ethen-1-yl)-3-difluoromethoxy-thiophene-2-carboxanilide in the form of a solid substance of melting point 80 to 82° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06319940B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-6b559aa5e99f45c7ac2505d15179bda8 |
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| Source note | uspto-grants-2001_11 |
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