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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246172Generated: October 30, 2026

Trifluoroacetic acid → 1-((R)-2-amino-3-methoxy-propionyl)-azetidine-3-carbonitrile trifluoroacetate

https://huagongshe.com/reaction/246172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant[(R)-2-(3-cyano-azetidin-1-yl)-1-methoxymethyl-2-oxo-ethyl]-carbamic acid tert-butyl esterHCID 71280690—
SolventDichloromethaneHCID 6344—
Product1-((R)-2-amino-3-methoxy-propionyl)-azetidine-3-carbonitrile trifluoroacetateHCID 71280253—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 25 mL round-bottomed flask, [(R)-2-(3-cyano-azetidin-1-yl)-1-methoxymethyl-2-oxo-ethyl]-carbamic acid tert-butyl ester (286 mg, 1.00 mmol) was dissolved in dichloromethane (4 ml). The reaction was cooled to 0° C. and trifluoroacetic acid (1.2 ml, 15.6 mmol) was slowly added. The reaction mixture was stirred at room temperature for 3 h then concentrated to provide 1-((R)-2-amino-3-methoxy-propionyl)-azetidine-3-carbonitrile trifluoroacetate as a colorless viscous oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658646B2
Source datasetuspto-grants-2014_02
ORD IDord-7dfacb3eaa9445d8ba847f16be5125f4
Source noteuspto-grants-2014_02