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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637560Generated: October 30, 2026

Ethyl 3-bromopropionate → HCID 20257135, compound

https://huagongshe.com/reaction/637560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-bromopropionateHCID 68320—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(2-Amino-3,4-dimethoxyphenyl)ethan-1-oneHCID 20257133—
SolventTriethylamineHCID 8471—
ProductHCID 20257135HCID 20257135—

Reaction Conditions

Temperature135 °C

Reaction Steps

Triethylamine (19.4 g, 192 mM) was added to a mixture of 2'-amino-3',4'-dimethoxyacetophenone (25 g, 128 mM) and ethyl 3-bromopropionate (139 g, 770 mM), in a 250 mL flask (equipped with a large stirring bar, reflux condenser and nitrogen inlet). The pale solid which formed was stirred at 135° C. for 5 hours. The brown homogeneous oil which formed was then cooled to 10° C. and 200 mL of 2% NaHCO3 was added. The solution was then extracted with CHCl3 (3×100 mL), the organic layer washed with H2O (100 mL) and dried over MgSO4. Following filtration, the CHCl3 and most of the bromopropionate were removed under reduced pressure. The oily residue was charged onto a 10×75 cm, SilicAR CC-7 column (800 g, hexane packed) and eluted with 5 to 20% ethyl acetate/hexane, collecting 1 L fractions. Evaporation of fractions 7-9 gave purified 2'-(N-2-carbethoxyethylamino)-3',4'-dimethoxyacetophenone as a yellow oil (5.86 g, 15%); UV (EtOH) nm: 244 (ε29110), 284 (ε11480); MS (Probe) 295 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04556739
Source datasetuspto-grants-1985_12
ORD IDord-decae6df6e3845ec9a942313150f86ba
Source noteuspto-grants-1985_12