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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284703Generated: November 4, 2026

Water → HCID 90051744, compound

https://huagongshe.com/reaction/2284703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant3-BenzyloxyanilineHCID 92892—
Reactant(2S)-2-(((tert-butoxy)carbonyl)(methyl)amino)propanoic acidHCID 7009590—
Solvent4-MethylmorpholineHCID 7972—
SolventTetrahydrofuranHCID 8028—
SolventIsobutyl chloroformateHCID 62365—
ProductHCID 90051744HCID 9005174493.6%

Reaction Steps

To a solution of N-Boc-N-methyl-L-alanine (561 mg) in tetrahydrofuran (14 mL), isobutyl chloroformate (362 μL) and N-methylmorpholine (303 μL) were added under ice cooling, and the mixture was stirred at the same temperature for 30 minutes. To the reaction mixture, 3-benzyloxyaniline (500 mg) was added under ice cooling, and the mixture was stirred at room temperature for 30 minutes. To the reaction mixture, water and ethyl acetate were added. The organic layer was separated, washed with saturated aqueous sodium chloride, and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent, 100 to 70% hexane in ethyl acetate) to obtain (S)-tert-butyl (1-((3-(benzyloxy)phenyl)amino)-1-oxopropan-2-yl)(methyl)carbamate (E15, 903 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145415B2
Source datasetuspto-grants-2015_09
ORD IDord-7d45d6273f234fb1a891c73b329b3c81
Source noteuspto-grants-2015_09