HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 131710791, compound → HCID 131710790, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 131710791 | HCID 131710791 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 131710790 | HCID 131710790 | — |
Reaction Steps
The solution of 0.5 g of N-(4-nitro-o-tolyl)-4-chloro-α-methylhomophthalimide in 120 ml of ethyl acetate is hydrogenated over 2.0 g of Raney nickel (washed with water and ethanol) at 2.5 atm. and room temperature for 5 hours. It is filtered and the filtrate evaporated, to yield the N-(4-amino-o-tolyl)-4-chloro-α-methylhomophthalimide of the formula ##STR8## showing in the I.R.-spectrum bands at 1665 and 1710cm-1 and in the mass-spectrum the ion of 314/316.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04025505 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-fddb1cfb316a416384d830f3357c8e14 |
| Source note | uspto-grants-1977_05 |