HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993902Generated: October 30, 2026
Ethyl bromoacetate → [(3-Chloro-phenyl)-methyl-amino]-acetic acid ethyl ester
https://huagongshe.com/reaction/1993902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-chloro-N-methylaniline | HCID 138900 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | [(3-Chloro-phenyl)-methyl-amino]-acetic acid ethyl ester | HCID 68536230 | 64.2% |
Reaction Steps
To a solution of 3-chloro-N-methylaniline (0.50 g, 3.35 mmol) in ethanol (7 ml) were added sodium carbonate (0.53 g, 5.03 mmol) and ethyl bromoacetate (0.42 ml, 3.69 mmol). The resulting suspension was stirred at room temperature for 1 hour and was then heated at 100° C. for 15 min under microwave irradiation. The mixture was then cooled to room temperature, diluted with ether, and filtered. The filtrate was washed with 1 M aqueous hydrochloric acid, the phases separated, and the aqueous phase extracted with ether. The combined organic extracts were dried over sodium sulphate, filtered and concentrated in vacuo. The residue was purified by flash chromatography (SiO2: heptane/ethyl acetate=gradient 100:0-70:30) to yield a brown oil (0.49 g, 64%); MS (ISP): 230.3, 228.1 ([M+H]+.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652055B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-d44f30d20fe34b8a94fc1f82d97dc80c |
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| Source note | uspto-grants-2010_01 |
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