HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl isobutyrylacetate → Ethyl 3-amino-4-methyl-pent-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl isobutyrylacetate | HCID 81583 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl 3-amino-4-methyl-pent-2-enoate | HCID 59557418 | — |
Reaction Steps
Ethyl 4-methyl-3-oxopentanoate (4.5 mL, 27.9 mmol) and ammonium acetate (12.05 g, 156 mmol) in MeOH (50 mL) was stirred at room temperature overnight. The solvent was evaporated in vacuo and chloroform (50 mL) was added. The resulting solid was filtered and washed with chloroform (2×25 mL). The combined filtrate was washed with water (30 mL) and brine (30 mL), dried over Na2SO4, and concentrated in vacuo to give ethyl 3-amino-4-methylpent-2-enoate, which was carried onto the next step without further purification. MS ESI calc'd. for C8H15NO2 [M+1]+ 158. found 158.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09226922B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-3b22d0bf3e44402da0d74ede6ad1db6a |
| Source note | uspto-grants-2016_01 |