Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475537Generated: October 29, 2026

Ammonium Chloride → (S)-3-((S)-2-azido-1-hydroxyethyl)pyrrolidine-1-carboxylic acid t-butyl ester

https://huagongshe.com/reaction/475537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
Reactant(S)-(S)-3-Oxiranylpyrrolidine-1-carboxylic Acid t-Butyl EsterHCID 86664071—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product(S)-3-((S)-2-azido-1-hydroxyethyl)pyrrolidine-1-carboxylic acid t-butyl esterHCID 86666088103.5%

Reaction Steps

A solution of (S)—(S)-3-oxiranylpyrrolidine-1-carboxylic acid t-butyl ester (1.1 g, 4.9 mmol, 1.0 eq.), sodium azide (800 mg, 12.3 mmol, 2.5 eq.), and ammonium chloride (474 mg, 8.9 mmol) in MeOH (25 mL) was stirred at reflux overnight. The white solid residue obtained on removal of solvent was dissolved in EtOAc (25 mL) and washed with water and saturated aqueous NaCl (1×25 mL each). The organic layer was then dried over Na2SO4 and concentrated to yield (S)-3-((S)-2-azido-1-hydroxyethyl)pyrrolidine-1-carboxylic acid t-butyl ester (1.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637568B2
Source datasetuspto-grants-2014_01
ORD IDord-aa1f67c8d0774226893cdd6c9b4c07e9
Source noteuspto-grants-2014_01