HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275982Generated: October 31, 2026
Ethyl bromoacetate → ethyl N-[4-(2-hydroxyethyl)phenyl]aminoacetate
https://huagongshe.com/reaction/275982
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Aminophenethyl alcohol | HCID 66904 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl N-[4-(2-hydroxyethyl)phenyl]aminoacetate | HCID 10537054 | — |
Reaction Steps
To a solution of 4-aminophenethyl alcohol (25 g) in N,N-dimethylformamide (500 ml) were added potassium carbonate (30 g) and ethyl bromoacetate (24 ml), and the mixture was stirred for 16 hours at room temperature. Diethylamine (38 ml) was added to the reaction mixture, and the resulting mixture was stirred for 1 hour. The insoluble material was filtered off and the filtrate was concentrated in vacuo. To the residue was added diethyl ether, and the resulting insoluble material was filtered off. The filtrate was washed with 10% aqueous citric acid solution, a saturated aqueous sodium bicarbonate solution and brine subsequently, and dried over anhydrous magnesium sulfate. Removal of the solvent in vacuo gave ethyl N-[4-(2-hydroxyethyl)phenyl]aminoacetate (35.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06353025B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-f1654327eae24a53b8d749af4a3065c5 |
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| Source note | uspto-grants-2002_03 |
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