HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium thiocyanate → HCID 13768634, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Reactant | 2-Chlorobenzoyl chloride | HCID 69110 | — |
| Reactant | 3-Methyl-4-(1H-pyrrol-1-yl)benzenamine | HCID 6484696 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13768634 | HCID 13768634 | 95.4% |
Reaction Steps
In a manner similar to Douglas and Dains, J. Am. Chem. Soc., 56, 719 (1934), the reaction of 3.1 g (0.017 mole) of 2-chlorobenzoyl chloride with 1.3 g (0.017 mole) of ammonium thiocyanate and 3.0 g (0.017 mole) of 3-methyl-4-(1H-pyrrol-1-yl)aniline (compound of Example 2) in 100 ml of acetone produced 6.0 g of 2-chloro-N-[[[3-methyl-4-(1H-pyrrol-1-yl)phenyl]amino]thioxomethyl]benzamide (mp 134°-136° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04617316 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-55a3b57f5a374298bf0178d35e66b293 |
| Source note | uspto-grants-1986_10 |