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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268181Generated: November 2, 2026

Triphenylphosphine → 4-(1-t-Butoxycarbonylpiperidin-4-yloxy)-3-chloronitrobenzene

https://huagongshe.com/reaction/1268181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantNitrofunginHCID 12074—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDichloromethaneHCID 6344—
Product4-(1-t-Butoxycarbonylpiperidin-4-yloxy)-3-chloronitrobenzeneHCID 2218109880.4%

Reaction Steps

To a solution of 1-t-butoxycarbonyl-4-hydroxypiperidine (3.32 g), 2-chloro-4-nitrophenol (2.36 g) and triphenylphosphine (5.11 g) in dichloromethane (60 ml) was added dropwise diethyl azodicarboxylate (3.1 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 hexane/ethyl acetate=5/2 as an eluant to give the desired compound (3.90 g, yield 76%) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555556B1
Source datasetuspto-grants-2003_04
ORD IDord-e3401e9203ea4e4eb0ac65bd82de9025
Source noteuspto-grants-2003_04