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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268185Generated: November 1, 2026

2-Methyl-4-nitrophenol → tert-Butyl 4-(2-methyl-4-nitrophenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/1268185

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-4-nitrophenolHCID 7442—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-(2-methyl-4-nitrophenoxy)piperidine-1-carboxylateHCID 2218107572.7%

Reaction Steps

To a solution of 1-t-butoxycarbonyl-4-hydroxypiperidine (3.62 g), 2-methyl-4-nitrophenol (2.55 g) and triphenylphosphine (5.25 g) in dichloromethane (100 ml) was added dropwise diethyl azodicarboxylate (3.2 ml) in an ice bath and the mixture was stirred at room temperature for 18 hours. The reaction mixture was concentrated in vacuo. The residue was purified by chromatography on a silica gel column using dichloromethane as an eluant to give the crude desired compound (4.07 g) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555556B1
Source datasetuspto-grants-2003_04
ORD IDord-dcb99d196976440bb313d93cc85e56c1
Source noteuspto-grants-2003_04