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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615601Generated: November 1, 2026

Ethyl Acetate → HCID 86654951, compound

https://huagongshe.com/reaction/1615601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 67307282HCID 67307282—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86654951HCID 8665495135.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (2-cyano-4-trifluoromethylphenylamino)acetic acid tert-butyl ester 5B (11.7 g, 39.0 mmol) in anhydrous THF (60 mL) and anhydrous DMF (60 mL) at 0° C. was added potassium tert-butoxide (8.74 g, 78.0 mmol). The reaction mixture was stirred at 0° C. for 5 minutes and benzyl chloroformate 5C (10 g, 58.7 mmol) was added. The reaction mixture was stirred at room temperature for 4 hours. Ethyl acetate (500 mL) was added and the organic layer was washed with water and brine. The organic layer was dried over sodium sulfate. The organic solvent was evaporated under reduced pressure. The crude product was purified by flash column chromatography to provide 3-amino-1-benzyloxycarbonyl-5-trifluoromethylindole-2-carboxylic acid tert-butyl ester 5D (5.96 g, 13.7 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765757B2
Source datasetuspto-grants-2014_07
ORD IDord-55a414c7d5fd4b2d83182c4d76067077
Source noteuspto-grants-2014_07