HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isoamyl Nitrite → 5-Amino-2-chloro-4-fluorobenzoyl cyanide oxime sodium salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-(5-Amino-2-chloro-4-fluorophenyl)acetonitrile | HCID 23036747 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Amino-2-chloro-4-fluorobenzoyl cyanide oxime sodium salt | HCID 86742949 | — |
Reaction Steps
0.3 g of sodium in 20 ml of absolute ethanol is introduced, with stirring, into a three-necked flask. There are then added slowly dropwise at room temperature, with stirring, firstly 1.8 g of 5-amino-2-chloro-4-fluorobenzyl cyanide and subsequently 1.5 ml of isopentylnitrite. The reaction solution is stirred at room temperature for a further 15 hours, and afterwards concentrated by evaporation. The residue is is taken up in glacial acetic acid, stirred up and filtered to thus obtain 2.2 g of the sodium salt of 5-amino-2-chloro-4-fluorobenzoyl cyanide which melts at 263°-264° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04950777 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-4e67201b4716452ab14457a2de830eb2 |
| Source note | uspto-grants-1990_08 |