HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981270Generated: October 31, 2026
Water → Ethyl 4-(2-tert-butoxycarbonylcyclopropyl)-2,3,5trifluorobenzoate
https://huagongshe.com/reaction/981270
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | tert-Butyl acetate | HCID 10908 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | Ethyl 4-(2-carboxycyclopropyl)-2,3,5-trifluorobenzoate | HCID 15136262 | — |
| Product | Ethyl 4-(2-tert-butoxycarbonylcyclopropyl)-2,3,5trifluorobenzoate | HCID 15136263 | 68.1% |
Reaction Steps
In 10 ml of tert-butyl acetate was dissolved 1.00 g of ethyl 4-(2-carboxycyclopropyl)-2,3,5-trifluorobenzoate. To the resulting solution was added 0.2 ml of a 70% aqueous perchloric acid solution. The resulting mixture was stirred at room temperature for 1 hour. To the reaction mixture were added 40 ml of ethyl acetate and 20 ml of water in this order. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue obtained was purified by a column chromatography (eluant: n-hexane/toluene=1/1) to obtain 0.81 g (yield: 68.1%) of ethyl 4-(2-tert-butoxycarbonylcyclopropyl)-2,3,5trifluorobenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04990508 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-60dba68a860c4ecfb5e5e18c6ab3ac03 |
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| Source note | uspto-grants-1991_02 |
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