HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitrophenylacetonitrile → (3-Amino-phenyl)-acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitrophenylacetonitrile | HCID 12125 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | (3-Amino-phenyl)-acetonitrile | HCID 4847850 | — |
Reaction Steps
A correspondingly substituted benzyl cyanide of the formula Ve is nitrated in concentrated sulfuric acid. The formed 3-nitrobenzyl cyanide of the formula Vf is subsequently hydrogenated in the presence of a catalyst with hydrogen to obtain 3-aminobenzyl cyanide of the formula Vg. By treatment with isopentyl nitrite in the presence of sodium and ethanol, there is formed the Na salt of 3-aminobenzoyl cyanide oxime of the formula Vh, which is reacted with an ester of the formula VIII to obtain 3-aminophenoxime ether of the formula Va. This can be subjected to a condensation reaction, as described above, with the 3,4,5,6-tetrahydrophthalic anhydride of the formula II.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04824476 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-02621c5e76a04003bffbc14b35953a91 |
| Source note | uspto-grants-1989_04 |