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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436130Generated: November 2, 2026

Triphenylphosphine → (S)-2-Chloro-4-(1-amino)ethylpyridine

https://huagongshe.com/reaction/1436130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant4-((S)-1-azidoethyl)-2-chloropyridineHCID 86612616—
SolventOxolane--water (1/1)HCID 21881883—
Product(S)-2-Chloro-4-(1-amino)ethylpyridineHCID 5099925858.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

Triphenylphosphine (9.56 g) was added to a solution of 4-((S)-1-azidoethyl)-2-chloropyridine (4.44 g) in tetrahydrofuran-water (4:1, 50 mL), and the reaction solution was heated and stirred at 60° C. for two hours. The reaction solution was returned to room temperature, and the solvent was evaporated under reduced pressure. Chloroform and 5 N hydrochloric acid were added to the residue, and the aqueous layer was separated. The aqueous layer was made basic with 5 N sodium hydroxide. Chloroform was added to the reaction solution, and the organic layer was separated. The organic layer was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure to obtain the title compound (2.24 g). The property values of the compound are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618960B2
Source datasetuspto-grants-2009_11
ORD IDord-b387d1ad6ea247238838b69b09908834
Source noteuspto-grants-2009_11