HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180085Generated: November 1, 2026
Triethylamine → Ethyl 3-(3-ethoxy-3-oxopropanamido)-3-methylbutanoate
https://huagongshe.com/reaction/1180085
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 3-chloro-3-oxopropionate | HCID 118931 | — |
| Reactant | Ethyl 3-amino-3-methylbutanoate hydrochloride | HCID 15578558 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 3-(3-ethoxy-3-oxopropanamido)-3-methylbutanoate | HCID 25193721 | 97% |
Reaction Steps
Ethyl 3-amino-3-methylbutanoate hydrochloride (0.87 g, 4.79 mmol) was suspended on methylene chloride (12 mL) and triethylamine (1.4 mL, 2.1 eq.). The mixture was cooled to 0° C. and treated dropwise with ethyl 3-chloro-3-oxopropanoate (0.64 mL, 1.05 eq.). The reaction was kept at room temperature for 2 hours, diluted with methylene chloride, washed with 1 N HCl and then with 5% NaHCO3, dried over Na2SO4 and evaporated to dryness to obtain ethyl 3-[(3-ethoxy-3-oxopropanoyl)amino]-3-methylbutanoate (1.2 g, Y=97%) as a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07279575B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-abf86e69b8eb4286999f3d6bf40a9578 |
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| Source note | uspto-grants-2007_10 |
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