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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617297Generated: November 1, 2026

Triphenylphosphine → HCID 10637402, compound

https://huagongshe.com/reaction/617297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Methylpyridin-3-olHCID 70719—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(S)-(-)-N-Boc-prolinolHCID 643448—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10637402HCID 1063740250%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of triphenylphosphine (3.83 g, 14.6 mmol) in 40 mL of anhydrous THF at 0° C. was added diethyl azodicarboxylate (2.30 mL, 14.6 mmol) dropwise. The mixture was stirred at 0° C. for 30 minutes, then brought to room temperature. (S)-1-t-Butoxycarbonyl-2-pyrrolidinemethanol (1.96 g, 9.75 mmol, Aldrich Chemical Co.) and 2-methyl-3-hydroxypyridine (Aldrich Chemical Co., 1.60 g, 14.6 mmol) were added to the reaction vessel, and the mixture was stirred for 16 hours. Solvent was removed in vacuo, and the residue was diluted with hexane and sonicated for 30 minutes. The resulting precipitate was filtered and washed with hexane. The hexane was removed in vacuo. The residue was purified by silica gel flash chromatography (ethyl acetate) to give 1.42 g (50% yield) of the title compound as a pale yellow oil. TLC Rf =0.50 (EtOAc). MS (DCI/NH3) m/e: 293 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05948793
Source datasetuspto-grants-1999_09
ORD IDord-987d1c35ac46416888b1fa0dbc3c28c1
Source noteuspto-grants-1999_09