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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424317Generated: October 31, 2026

Hydrochloric Acid → Methyl (2S)-2-amino-3-(4-bromophenyl)propanoate

https://huagongshe.com/reaction/1424317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant4-Bromo-L-phenylalanineHCID 671214—
ProductMethyl (2S)-2-amino-3-(4-bromophenyl)propanoateHCID 24720903—

Reaction Steps

1.0 g (4.01 mmol) H-Phe(4-Br)—OH were refluxed in 20 ml methanol with 2.1 ml HCl (4 M in 1,4-dioxane) over night. Evaporation of the solvent gave H-Phe(4-Br)—OMe*HCl as white solid. 1.0 g (3.4 mmol) of this hydrochloride and 1.7 ml (10.2 mmol) DIPEA were suspended in 8 ml THF and 0.41 ml (3.4 mmol) 2,4,6-trimethylbenzoyl chloride were added dropwise at 0° C. After 18 h at room temperature the reaction was quenched with water and the solvent was removed. The residue was suspended in ethyl acetate, washed with saturated Na2SO4 and brine to give compound (13) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927534B2
Source datasetuspto-grants-2015_01
ORD IDord-89c55b79e431430383c54221e7ef7434
Source noteuspto-grants-2015_01