HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637560Generated: October 30, 2026
Ethyl 3-bromopropionate → HCID 20257135, compound
https://huagongshe.com/reaction/637560
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 3-bromopropionate | HCID 68320 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(2-Amino-3,4-dimethoxyphenyl)ethan-1-one | HCID 20257133 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 20257135 | HCID 20257135 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04556739 |
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| Source dataset | uspto-grants-1985_12 |
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| ORD ID | ord-decae6df6e3845ec9a942313150f86ba |
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| Source note | uspto-grants-1985_12 |
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