HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 23325158, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 23325179 | HCID 23325179 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Product | HCID 23325158 | HCID 23325158 | — |
Reaction Steps
0.8 g of Raney-nickel are placed in a hydrogenation flask and suspended in 50 ml of ethanol. 7.6 g of 4'-chloro-2,2'-diethoxy-2'-nitroacetanilide are added thereto and the mixture is hydrogenated at room temperature and normal pressure. The uptake of hydrogen has finished after 2 hours. After suction filtration and concentration of the filtrate, the product is precipitated with water. There is obtained 4'-chloro-2,2-diethoxy-2'-aminoacetanilide of melting point 89°-90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04582526 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-58fab68b9f434f7d80479eed8b844d08 |
| Source note | uspto-grants-1986_04 |