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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180075Generated: November 1, 2026

Diphosgene → 4-Phenyl-piperidine-1-carboxylic acid 4-(5-methyl-pyridin-2-ylmethyl)-phenyl ester

https://huagongshe.com/reaction/1180075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphosgeneHCID 10426—
Reactant4-PhenylpiperidineHCID 69873—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(5-Methyl-pyridin-2-ylmethyl)phenolHCID 22047848—
SolventDichloromethaneHCID 6344—
Product4-Phenyl-piperidine-1-carboxylic acid 4-(5-methyl-pyridin-2-ylmethyl)-phenyl esterHCID 6951796928%

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 4-(5-methyl-pyridin-2-ylmethyl)phenol (0.8 mmol) prepared as described above and ethyldiisopropylamine (1.5 mmol) in CH2Cl2 (5 mL) at −30° C. was added trichloromethyl chloroformate (1.0 mmol). The solution was stirred at −30° C. for 10 min and at reflux temperature for 2 h. The solution was evaporated to dryness and redissolved in CH2Cl2 (5 mL) and cooled to 0° C. before addition of 4-phenylpiperidine (1.5 mmol). The solution was stirred at room temperature for 16 h evaporated to give the crude product which was purified by FC (Quad flash 40 CH2Cl2:Et2O:Heptane:Et3N 1:1:2:0.25->1:1:1:0.25) to give the title compound in 28% yield as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279470B2
Source datasetuspto-grants-2007_10
ORD IDord-cfb4e9480a7c4414861481fc4c3c9059
Source noteuspto-grants-2007_10