Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007569Generated: October 25, 2026

Triethylamine → n-Formyl-l-leucine tert-butyl ester

https://huagongshe.com/reaction/1007569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(Formyloxy)acetonitrileHCID 4205685—
Reactanttert-butyl (2S)-2-amino-4-methylpentanoate hydrochlorideHCID 12451443—
SolventDichloromethaneHCID 6344—
Productn-Formyl-l-leucine tert-butyl esterHCID 11160222—

Reaction Steps

The preparation was performed in analogy to W. Duczek et al., Synthesis, 37-38 (1996). A solution of 4.04 g (40 mmol) of triethylamine in 10 mL of dichloromethane was added to a solution of 8.94 g (40 mmol) of L-leucine tert-butyl ester hydrochloride and 3.4 g (40 mmol) of cyanomethyl formate in 60 mL of dichloromethane at 0° C. The reaction solution was allowed to warm to room temperature, stirred at room temperature overnight, and then washed twice with saturated NaCl solution. The phases were separated and the organic phase was dried over magnesium sulfate. The residue obtained after filtration and removal of the solvent in vacuo was distilled in vacuo. Yield: 7.5 g (87%). Boiling point: 118° C./2.7 Pa (0.02 torr).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794517B2
Source datasetuspto-grants-2004_09
ORD IDord-9e9028be0e544e89848222ce1c80d7fa
Source noteuspto-grants-2004_09