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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617298Generated: October 31, 2026

Triphenylphosphine → HCID 54565828, compound

https://huagongshe.com/reaction/617298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Methyl-5-hydroxypyridineHCID 14275—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(S)-(-)-N-Boc-prolinolHCID 643448—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54565828HCID 5456582857%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of triphenylphosphine (3.83 g, 14.60 mmol) in 40 mL of anhydrous THF at 0° C. was added diethyl azodicarboxylate (2.3 mL, 14.60 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 6-methyl-3-pyridinol (Aldrich Chemical Co., 1.60 g, 14.60 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 using a gradient from 100% hexane to a 1:1 solution of ethyl acetatelh exane (100%Hex, 10% EtOAc/Hex, 20%EtOAc/Hex, 1:1EtOAc/Hex) to give 1.61 g (57% ) of the title compound as a pale yellow oil. TLC Rf=0.42 (1:1 EtOAc/Hex). 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-64094540a9764c61ab4f91352af4ff59
Source noteuspto-grants-1999_09