Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861912Generated: November 2, 2026

Dichloromethane → Phenylalanine, N-t-butyloxycarbonyl-4-nitro-, t-butyl ester

https://huagongshe.com/reaction/1861912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactanttert-ButanolHCID 6386—
Reactant2-tert-Butoxycarbonylamino-3-(4-nitro-phenyl)-propionic acidHCID 118071—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventEthyl AcetateHCID 8857—
ProductPhenylalanine, N-t-butyloxycarbonyl-4-nitro-, t-butyl esterHCID 54650397%

Reaction Steps

To a mixture of the compound (6.9 g) obtained in Example 63 and methylene chloride (70 ml) were added t-butanol (20 ml), N,N-dimethylaminopyridine (2.63 g) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (4.9 g) and the resulting mixture was stirred at room temperature for 4 days. The reaction mixture was diluted with ethyl acetate and washed successively with 2 N HCl and a saturated aqueous sodium chloride solution; the organic layer was dried with anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent, n-hexane:ethyl acetate=3:1) to give 7.64 g of the titled compound (yield, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06534546B1
Source datasetuspto-grants-2003_03
ORD IDord-ff96db7c8e374413b724973db09f5f77
Source noteuspto-grants-2003_03