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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378387Generated: November 2, 2026

Phthalimide → HCID 70204323, compound

https://huagongshe.com/reaction/1378387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 70204259HCID 70204259—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70204323HCID 7020432385.2%

Reaction Steps

In 250 ml of absolute tetrahydrofuran, is dissolved 8.0 g (26.4 mmol) of trans-1-benzyloxycarbonyl-3-hydroxymethyl-4-trifluoromethylpyrrolidine. To the above solution, are added 4.27 g (29.0 mmol) of phthalimide and 8.30 g (31.7 mmol) of triphenylphosphine. Further, 5.0 ml (31.7 mmol) of azo dicarboxylic acid diethyl ester is added dropwise to the above solution on cooling with ice. After stirring at room temperature for 3 hours, the reaction mixture was concentrated under reduced pressure, and diethyl ether was added to the concentrated mixture to give a precipitate. The resulting precipitate was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified with silica gel column chromatography (elusion solvent; chloroform/n-hexane (4/1→8/1)) to give 9.72 g of the objective substance as a colorless powder (yield 85.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05668147
Source datasetuspto-grants-1997_09
ORD IDord-4da255477fc04024aec64f62cfed224b
Source noteuspto-grants-1997_09