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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661229Generated: November 2, 2026

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

https://huagongshe.com/reaction/661229

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 the compound from Example 2A 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 numberUS08084469B2
Source datasetuspto-grants-2011_12
ORD IDord-d390e9867f254faebe3297aa431df4ea
Source noteuspto-grants-2011_12