HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 19086746, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | HCID 19086749 | HCID 19086749 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19086746 | HCID 19086746 | — |
Reaction Steps
Glacial acetic acid (40cm3) containing concentrated sulphuric acid (3 drops) was added to a stirred mixture of 4-(2-chloro-4-trifluoromethyl-6-fluorophenoxy)-2-nitroaniline (1 g), paraformaldehyde (0.26 g), anhydrous zinc chloride (1.43 g) and potassium cyanide (0.56 g). The resulting suspension was heated at 50°-55° C. for 7.5 hours and left to stand at room temperature overnight. The mixture was poured into water and extracted with ethyl acetate (×2). The combined organic phase was washed with water, dried (MgSO4), and filtered. The solvent was removed from the filtrate under vacuum to give 4-(2-chloro-4-trifluoromethyl-6-fluorophenoxy)-2-nitro-N-cyanomethylaniline (0.82 g) as an orange solid. M+ =389.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05306692 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-829e40cb308a48e5850f82d32ef6d4e2 |
| Source note | uspto-grants-1994_04 |