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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269535Generated: October 27, 2026

Imidazole-1-carboxylic acid 4-trifluoromethylbenzyl ester → 3-[3-(1-Ethoxycarbonyl-1-methyl-ethoxy)-4-methyl-phenyl]-piperidine-1-carboxylic acid 4-trifluoromethyl-benzyl ester

https://huagongshe.com/reaction/1269535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazole-1-carboxylic acid 4-trifluoromethylbenzyl esterHCID 68882567—
Reactant2-Methyl-2-(2-methyl-5-piperidin-3-yl-phenoxy)-propionic acid ethyl ester l-tartaric acid saltHCID 68884638—
SolventEthyl AcetateHCID 8857—
Product3-[3-(1-Ethoxycarbonyl-1-methyl-ethoxy)-4-methyl-phenyl]-piperidine-1-carboxylic acid 4-trifluoromethyl-benzyl esterHCID 6888685091%

Reaction Steps

2-methyl-2-(2-methyl-5-piperidin-3-yl-phenoxy)-propionic acid ethyl ester L-tartaric acid salt (Example 11; 155 mg, 0.34 mmol) was dissolved in 50 mL ethyl acetate and washed with 50 mL saturated aqueous NaHCO3. The organic phase was dried over Na2SO4 and concentrated under reduced pressure. The resultant oil was taken up in 3 mL toluene and imidazole-1-carboxylic acid 4-trifluoromethyl-benzyl ester (92 mg, 0.34 mmol) was added. The reaction was stirred for 18 h at room temperature under nitrogen. The reaction was flash chromatographed with 15% ethyl acetate/hexanes to yield 157 mg (91%) of the desired 3-[3-(1-ethoxycarbonyl-1-methyl-ethoxy)-4-methyl-phenyl]-piperidine-1-carboxylic acid 4-trifluoromethyl-benzyl ester as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199243B2
Source datasetuspto-grants-2007_04
ORD IDord-a4f4db91668049c393a02b347ba920f2
Source noteuspto-grants-2007_04