Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | HCID 22717937 | HCID 22717937 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22717973 | HCID 22717973 | 62% |
Reaction Steps
The monoethyl 2-(4-benzyloxycarbonylaminobutyl)malonate (3.03 g) obtained in the above step (d) was cooled to 0° C. and added with 36% formaldehyde solution (3 ml) and then with diethylamine (3 ml), and then the mixture was stirred at room temperature for 19.5 hours. Ethyl acetate was added to the reaction system to extract the organic substances, and the organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (150 g, hexane:acetone=5:1) to obtain ethyl 2-(4-benzyloxycarbonylaminobutyl)acrylate (1.69 g, 62%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06576627B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-b94780af395d4f9197bf01282ccf9d2c |
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| Source note | uspto-grants-2003_06 |
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