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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620932Generated: October 31, 2026

Benzyl chloroformate → HCID 57446950, compound

https://huagongshe.com/reaction/1620932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
Reactant5,5,5-trifluoro-l-leucineHCID 164587—
SolventWaterHCID 962—
ProductHCID 57446950HCID 57446950—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of the 5,5,5-trifluoro-L-leucine (12 g) in H2O (150 mL) at 0° C. was added benzyl chloroformate (4.8 mL, 34 mol), followed by dropwise addition of 1 M aqueous NaOH (120 mL, 120 mmol). More benzyl chloroformate (4.8 mL, 34 mmol) was added. The mixture was further stirred at 0° C. and the pH of the mixture became ˜7. The mixture was washed with Et2O (2×) and acidified with aqueous HCl. The aqueous layer was extracted with EtOAc (3×), dried (Na2SO4) and concentrated in vacuo to provide N-[(benzyloxy)carbonyl]-5,5,5-trifluoro-L-leucine. The crude acid was dissolved in Et2O and treated with a solution of diazomethane in Et2O. Chromatography over silica gel and elution with hexanes:Et2O (7:3) gave methyl (4S)—N—[(benzyloxy)carbonyl]-5,5,5-trifluoro-L-leucinate as the less polar fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772336B2
Source datasetuspto-grants-2014_07
ORD IDord-5eebd26c9b634322a65f69aa75bec215
Source noteuspto-grants-2014_07