HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35267Generated: October 26, 2026
Hydrochloric Acid → 4-Hydroxy-3-(4-trifluoromethyloxyphenyl-carbamoyl)-coumarin
https://huagongshe.com/reaction/35267
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-(Trifluoromethoxy)phenyl isocyanate | HCID 92298 | — |
| Reactant | 4-Hydroxycoumarin | HCID 54682930 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Hydroxy-3-(4-trifluoromethyloxyphenyl-carbamoyl)-coumarin | HCID 54693881 | 45.6% |
Reaction Steps
First 5.1 g (0.05 mol) of triethylamine and then, slowly, 10.2 g (0.05 mol) of 4-trifluoromethoxyphenyl isocyanate are added dropwise to 8.1 g (0.05 mol) of 4-hydroxycoumarin in 100 ml of dimethylsulphoxide at room temperature. The temperature thereby rises to 31° C. The reaction mixture is subsequently stirred at room temperature for 5 hours. It is added to a mixture of 250 ml of cold water and 15 ml of concentrated hydrochloric acid, whereupon a white precipitate separates out. The mixture is stirred for 30 minutes, with cooling, and the precipitate is filtered off with suction, rinsed with acid water and dried at 50° C. in vacuo. Recrystallization from 100 ml of dioxane gives 8.3 g (45.6% of theory) of 4-hydroxy-3-(4-trifluoromethyloxyphenyl-carbamoyl)-coumarin of melting point 194°-195° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766144 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-268688d9dcef4871bc52a521b549d8f2 |
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| Source note | uspto-grants-1988_08 |
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