Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260910Generated: November 1, 2026

Water → N-benzyl-N-[2-(3,4-dichlorophenyl)-3-ethoxy-3-oxopropyl]-beta-alanine ethyl ester

https://huagongshe.com/reaction/1260910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 68870857HCID 68870857—
SolventAcetonitrileHCID 6342—
ProductN-benzyl-N-[2-(3,4-dichlorophenyl)-3-ethoxy-3-oxopropyl]-beta-alanine ethyl esterHCID 6887048199.7%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a solution of the compound (27.8 g) obtained in step 2 and sodium carbonate (16.3 g) in acetonitrile (132 mL) was added benzyl bromide (14.4 g) at room temperature, and the mixture was stirred at 75° C. for 2 hr. The reaction mixture was poured into water, and the resultant product was extracted with ethyl acetate. The organic layer was washed with brine and dried, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (solvent gradient; 5→20% ethyl acetate/hexane) to give N-benzyl-N-[2-(3,4-dichlorophenyl)-3-ethoxy-3-oxopropyl]-β-alanine ethyl ester (34.6 g, 99%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470816B2
Source datasetuspto-grants-2013_06
ORD IDord-df46ca8bab8d4b79af72de0cbc037774
Source noteuspto-grants-2013_06