HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 178492221, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | HCID 12551428 | HCID 12551428 | — |
| Product | HCID 178492221 | HCID 178492221 | — |
Reaction Steps
4,5-dihydro-1-phenylmethyl-1H-pyrazol-3-amine (24 g) (prepared by the method of H. Dorm, A. Otto, Chem Ber. 103 2505 (1970), p-anisidine (17.5 g) and p-toluenesulphonic acid (100 mg) was heated at 170° under dry nitrogen until evolution of ammonia ceased. The reaction mix was cooled, purified by chromatography on SiO2 eluting with ether:pentane 1:1 to give the sub-title compound as colourless cubes (13.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04803216 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-e5197466db174aa6bfde8a395e4826b4 |
| Source note | uspto-grants-1989_02 |