HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-(3-chlorophenyl)-4-nitrobutanoate → Ethyl 4-amino-3-(3-chlorophenyl)butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-(3-chlorophenyl)-4-nitrobutanoate | HCID 22387109 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-amino-3-(3-chlorophenyl)butanoate | HCID 22387061 | 78% |
Reaction Steps
In a 2 L pressure jar, under inert atmosphere, 196 g (733 mmoles) of ethyl 3-(3-chlorophenyl)-4-nitrobutanoate 377 are dissolved in 200 ml of ethanol. A suspension of 200 g of predried (3×, ethanol) Raney Nickel in 700 ml of ethanol is added and the mixture hydrogenated on a Parr hydrogenator at a maximum of 20 psi H2 pressure (STRONGLY EXOTHERMIC REACTION, ice/water cooling required). The mixture is degassed, filtered on a Celite/Norite pad, and the filtrate concentrated in vacuo, to give 136.7 g of crude 378, 78% yield, used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07692028B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-8c10361273034275a2a734d2f216bd33 |
| Source note | uspto-grants-2010_04 |