HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29061Generated: October 27, 2026
Ethyl bromoacetate → (s)-[But-3-enyl-(1-phenyl-ethyl)-amino]-acetic acid ethyl ester
https://huagongshe.com/reaction/29061
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | But-3-enyl-((S)-1-phenyl-ethyl)-amine | HCID 10559173 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (s)-[But-3-enyl-(1-phenyl-ethyl)-amino]-acetic acid ethyl ester | HCID 10956339 | 94.5% |
Reaction Steps
To a solution of But-3-enyl-((S)-1-phenyl-ethyl)-amine (6.37 g, 36.4 mmol) in 150 mL of DMF at 0° C. is added K2CO3 (10.0 g, 72.8 mmol) in small portions. After stirring at 0° C. for 10 min, ethylbromoacetate (8.35 g, 54.6 mmol) izs added slowly. The reaction mixture, a white suspension, is stirred at r.t. overnight/16 hrs. The solution is diluted with 200 mL of ether, and washed with 3×100 ml of water. The crude product is purified by chromatography (hexane/CH2Cl2: 50/50) to give a pale liquid(8.5 g, 94.5%). (NMR and MS data confirmed, U-4117-58).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07419975B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-ba3faff163924c36bd90fcaa1113892f |
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| Source note | uspto-grants-2008_09 |
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