HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Aminoacetophenone → 1-(4-Methylphenyl)-2-oxo-3-pyrrolidinecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Aminoacetophenone | HCID 7468 | — |
| Reactant | 6,6-Dimethyl-5,7-dioxaspiro(2.5)octane-4,8-dione | HCID 79720 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-Methylphenyl)-2-oxo-3-pyrrolidinecarboxylic acid | HCID 3362315 | 246.8% |
Reaction Steps
This compound was prepared according to general method 1 starting from 6,6-dimethyl-5,7-dioxaspiro[2.5]octane-4,8-dione (0.500 g, 2.94 mmol) and 1-(4-aminophenyl)ethanone (1.19 g, 1.19 mmol) in ethanol (3 mL). 2-oxo-1-p-tolylpyrrolidine-3-carboxylic acid 0.644 g (quantitative) was obtained as a bright yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08618138B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-81deef5a716d4ffbac81098960dc0466 |
| Source note | uspto-grants-2013_12 |