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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268232Generated: October 30, 2026

Triphenylphosphine → HCID 18542735, compound

https://huagongshe.com/reaction/1268232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantHCID 18542712HCID 18542712—
SolventDichloromethaneHCID 6344—
ProductHCID 18542735HCID 1854273593.7%

Reaction Steps

To a solution of 1-t-butoxycarbonyl-4-hydroxypiperidine (5.4 g), methyl 4-methyl-5-nitrosalicylate (2.8 g) and triphenylphosphine (9.0 g) in dichloromethane (100 ml) was added diethyl azodicarboxylate (5.4 ml) and the mixture was stirred at room temperature for 9 hours. The reaction mixture was concentrated in vacuo. The residue was purified by chromatography on a silica gel column using hexane/ethyl acetate=4/1 as an eluant to give the desired compound (4.9 g, yield 93%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555556B1
Source datasetuspto-grants-2003_04
ORD IDord-ab45f4ba28eb444088ddc074c5c376e7
Source noteuspto-grants-2003_04