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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactanttert-Butyl acetateHCID 10908—
ReactantPerchloric AcidHCID 24247—
ReactantEthyl 4-(2-carboxycyclopropyl)-2,3,5-trifluorobenzoateHCID 15136262—
ProductEthyl 4-(2-tert-butoxycarbonylcyclopropyl)-2,3,5trifluorobenzoateHCID 1513626368.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04990508
Source datasetuspto-grants-1991_02
ORD IDord-60dba68a860c4ecfb5e5e18c6ab3ac03
Source noteuspto-grants-1991_02