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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799303Generated: October 25, 2026

Acetic Acid Mixture with Hydrobromic Acid → 2-({(2S)-2-amino-3-[4-(trifluoromethoxy)phenyl]propanoyl}amino)ethyl acetate

https://huagongshe.com/reaction/1799303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic Acid Mixture with Hydrobromic AcidHCID 21893785—
Reactantbenzyl (1S)-2-[(2-hydroxyethyl)amino]-2-oxo-1-[4-(trifluoromethoxy)benzyl]ethylcarbamateHCID 86636534—
SolventAcetic AcidHCID 176—
Product2-({(2S)-2-amino-3-[4-(trifluoromethoxy)phenyl]propanoyl}amino)ethyl acetateHCID 6901754380.1%

Reaction Steps

A 30% hydrogen bromide acetic acid solution (13.1 mL, 65.9 mmol) was added to an acetic acid (4.4 mL) solution of benzyl (1S)-2-[(2-hydroxyethyl)amino]-2-oxo-1-[4-(trifluoromethoxy)benzyl]ethylcarbamate (9.36 g, 22.0 mmol) prepared in Reference Example 6 (6b) under ice-cooling with stirring. The mixture was stirred at room temperature for 4 hours, and then ice water (300 mL) was added thereto. The reaction solution was washed with diethyl ether (50 mL, three times), and subsequently the water layer was neutralized with sodium bicarbonate (about 40 g) and extracted with methylene chloride (300 mL, three times). The organic layer was dried over anhydrous sodium sulfate, and the solvent was evaporated. The residue was dried under reduced pressure to give 5.89 g of the title compound (yellow solid, yield: 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344029B2
Source datasetuspto-grants-2013_01
ORD IDord-a8be4f79b09f4eccbee424ec15999990
Source noteuspto-grants-2013_01