HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Ethyl 3-amino-3-[1-(4-chlorophenyl)cyclobutyl]propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Ethyl 3-amino-3-[1-(4-chlorophenyl)cyclobutyl]acrylate | HCID 67945594 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-amino-3-[1-(4-chlorophenyl)cyclobutyl]propanoate | HCID 19823680 | — |
Reaction Steps
A solution of ethyl 3-amino-3-[1-(4-chlorophenyl)-cyclobutyl]acrylate (90 g), sodium cyanoborohydride (36 g), ammonium acetate (27 g) and acetic acid (60 ml) in ethanol (1.5 litres) was allowed to stand at room temperature for 5 days and then concentrated to 600 ml and poured into water (2.5 litres). The aqueous solution was basified, extracted with ether and the ether extract back extracted with 2N hydrochloric acid. The acidic aqueous extract was cooled with ice, basified and extracted with ether and the extract dried and evaporated to give ethyl 3-amino-3-[1-(4-chlorophenyl)cyclobutyl]propanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05047432 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-8d5fbb128b3743be8ba0ecd4b8913597 |
| Source note | uspto-grants-1991_09 |