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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242103Generated: November 2, 2026

Phthalimide → HCID 11293501, compound

https://huagongshe.com/reaction/1242103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant4,4-diethoxy-1-((S)1-phenyl-ethyl)-(R)-2-hydroxymethyl-piperidineHCID 11771237—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11293501HCID 1129350172,485.797%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4,4-Diethoxy-1-((S)1-phenyl-ethyl)-(R)-2-hydroxymethyl-piperidine (65.35 g, 0.213 mmol), triphenylphosphine (61.3 g, 0.234 mol) and phthalimide (34.4 g, 0.234 mol), in tetrahydrofuran (700 ml) cooled to 0° C. was added diethyl azodicarboxylate over the course of 1.5 hour. The reaction mixture was stirred at 0° C. for another 2 hours before the solvent was removed in vacuo. The residue was dissolved in hot heptane-toluene (3:2) (650 ml) before it was cooled on an ice bath. The precipitate consisting of triphenyl phosphine oxide was filtered off and washed with heptane. The filtrate was concentrated in vacuo and the residue subjected to column chromatography using a mixture of toluene-ethyl acetate-heptane (3:1:3) as eluent. The solvent was evaporated in vacuo whereupon a viscous oil was obtained. Upon addition of light petrol ether the product crystallized to give 67.4 g (73%) of the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115624B1
Source datasetuspto-grants-2006_10
ORD IDord-9db71dd7bbba4adfbb7675274327f5fb
Source noteuspto-grants-2006_10