HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Ethyl 3-allyloxycarbonylamino-3-(3-aminophenyl)-propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Ethyl 3-allyloxycarbonylamino-3-(3-nitrophenyl)-propionate | HCID 21101502 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-allyloxycarbonylamino-3-(3-aminophenyl)-propionate | HCID 21101501 | 76.8% |
Reaction Steps
64.6 g of tin-(II) chloride were added to a solution of 18.8 g of ethyl 3-{[(allyloxy)-carbonyl]-amino}-3-(3-nitrophenyl)-propanoate from Example II.2.c in 245 ml of ethanol, and the mixture was heated to reflux for 2 h. The reaction mixture was hydrolized with 300 ml of aqueous 2N sodium hydroxide solution, then filtered through silica gel, and the filtrate was washed with dichloromethane. The organic phase was dried over magnesium sulphate and concentrated to yield 13.1 g of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07304037B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-42f615a4b778435dbb31ca493940e88a |
| Source note | uspto-grants-2007_12 |