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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222592Generated: October 26, 2026

1,1'-Carbonyldiimidazole → 1-(1-Trifluoromethyl-cyclopropanecarbonyl)-piperidine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/222592

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
Reactant1-(Trifluoromethyl)cyclopropane-1-carboxylic acidHCID 2778306—
SolventTetrahydrofuranHCID 8028—
Product1-(1-Trifluoromethyl-cyclopropanecarbonyl)-piperidine-4-carboxylic acid ethyl esterHCID 66865273102.2%

Reaction Steps

1,1′-Carbonyldiimidazole (77.36 g; 467.52 mmol) is added to a solution of 1-(trifluoromethyl)cyclopropanecarboxylic acid (72.04 g; 467.52 mmol) in tetrahydrofuran (600 mL) while keeping the internal temperature below 30° C. Piperidine-4-carboxylic acid ethyl ester (50 g; 311.68 mmol) is added after 10 min and the reaction is stirred under nitrogen atmosphere at room temperature for 16 h. The solvent is removed under controlled vacuum and the residue is partitioned between 2 M aqueous solution of sodium hydroxide (200 mL) and dichloromethane (300 mL). The organic layer is washed with brine (100 mL), dried over magnesium sulphate, filtered and concentrated to obtain 93.45 g of the title compound. MS (m/z) 294 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207344B2
Source datasetuspto-grants-2012_06
ORD IDord-7b121c550df14e8fa59c5e078c988145
Source noteuspto-grants-2012_06