Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900085Generated: November 1, 2026

Pyridine → t-Butyl 4-(4-ethoxycarbonylamino-phenyl)-piperidine-1-carboxylate

https://huagongshe.com/reaction/1900085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl chloroformateHCID 10928—
Reactanttert-Butyl 4-(4-aminophenyl)piperidine-1-carboxylateHCID 21940085—
SolventDichloromethaneHCID 6344—
Productt-Butyl 4-(4-ethoxycarbonylamino-phenyl)-piperidine-1-carboxylateHCID 2337187155.2%

Reaction Steps

8.84 g (32.0 mmol) of t-butyl 4-(4-aminophenyl)-piperidine-1-carboxylate were dissolved in 150ml of methylene chloride and treated with 3.82 g (35.2 mmol) of ethyl chloroformate in the presence of 2.78 g (35.2 mmol) of pyridine. The reaction mixture was stirred at room temperature for 16 hours. Thereafter, it was washed with water and the organic phase was dried over sodium sulfate, filtered and evaporated. The residue (11.3 g) was chromatographed on 95 g of silica gel 60 with ether/n-hexane (4:6). After recrystallization from ether/n-hexane there were obtained 6.15 g of t-butyl 4-(4-ethoxycarbonylamino-phenyl)-piperidine-1-carboxylate. M.p.: 126°-128°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574055
Source datasetuspto-grants-1996_11
ORD IDord-f9830ce84748488ea495eb73b0c0a207
Source noteuspto-grants-1996_11