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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020339Generated: November 1, 2026

Ethyl 2-(1-piperidinyl)-4-trifluoromethyloxazole-5-carboxylate → HCID 57461778, compound

https://huagongshe.com/reaction/1020339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(1-piperidinyl)-4-trifluoromethyloxazole-5-carboxylateHCID 57461777—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductHCID 57461778HCID 57461778100.2%

Reaction Steps

To a solution of ethyl 2-(1-piperidinyl)-4-trifluoromethyloxazole-5-carboxylate (A-3) (1.28 g) in THF (20 mL) at RT was added 1 N NaOH (20 mL). The reaction mixture was stirred at RT for 3 h then diluted with H2O (100 mL) and 1 N NaOH (10 mL). The aqueous solution was washed with Et2O (2×100 mL) and then acidified to pH=1 by addition of 1 N HCl, and extracted with EtOAc (3×50 mL). The combined organic extract was dried over Na2SO4, filtered, and concentrated to yield 2-(1-piperidinyl)-4-trifluoromethyloxazole-5-carboxylic acid (A-4) as a white solid (1.16 g, 100% yield). LCMS (ESI) calcd for [M+1]+ 265.1. found 265.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716312B2
Source datasetuspto-grants-2014_05
ORD IDord-a6ddf7d4afcd4dd78a8407c39f6a1816
Source noteuspto-grants-2014_05