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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091744Generated: October 31, 2026

Triethylamine → 3-Methyl 1-(4-nitrophenyl) 5-[4-(trifluoromethyl)phenyl]piperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/2091744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantMethyl 5-(4-(trifluoromethyl)phenyl)piperidine-3-carboxylateHCID 58002265—
SolventDichloromethaneHCID 6344—
Product3-Methyl 1-(4-nitrophenyl) 5-[4-(trifluoromethyl)phenyl]piperidine-1,3-dicarboxylateHCID 58002325—

Reaction Conditions

Temperature0 °C

Reaction Steps

20.0 g (69.6 mmol) of methyl 5-[4-(trifluoromethyl)phenyl]piperidine-3-carboxylate (Example 13A) were dissolved in 1.0 l of dichloromethane, and admixed at 0° C. with 14.1 g (139 mmol) of triethylamine Subsequently, 14.0 g (69.6 mmol) of 4-nitrophenyl chlorocarbonate were added dropwise. The reaction mixture was stirred at 0° C. for 2 h and then at RT for 16 h. For workup, the mixture was washed with saturated aqueous sodium hydrogencarbonate solution. The organic phase was dried over magnesium sulphate, filtered and concentrated under reduced pressure. This gave 31.3 g of crude product, which was reacted without any further purification steps.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440657B2
Source datasetuspto-grants-2013_05
ORD IDord-df2483d00bfc43e08c14826da530e556
Source noteuspto-grants-2013_05