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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268213Generated: November 2, 2026

Triphenylphosphine → HCID 18542737, compound

https://huagongshe.com/reaction/1268213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantHCID 18542715HCID 18542715—
SolventDichloromethaneHCID 6344—
ProductHCID 18542737HCID 1854273779%

Reaction Steps

To a solution of 1-t-butoxycarbonyl-4-hydroxypiperidine (6.3 9), methyl 3-chloro-5-nitrosalicylate (2.4 g) and triphenylphosphine (10.8 g) in dichloromethane (100 ml) was added diethyl azodicarboxylate (6.6 ml) and the mixture was stirred at room temperature for 4 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 (3.4 g, yield 79%) as a pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555556B1
Source datasetuspto-grants-2003_04
ORD IDord-6fdd6729002c4f8f8e3217b43084e58d
Source noteuspto-grants-2003_04