HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-Methyl-N-(3,4-dichlorostyryl)acetamidine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl fluorosulfate | HCID 9870 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-methyl-N-(3,4-dichlorostyryl)acetamidine | HCID 53645811 | — |
| Reactant | HCID 178465601 | HCID 178465601 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Methyl-N-(3,4-dichlorostyryl)acetamidine hydrochloride | HCID 86735119 | — |
Reaction Steps
An alternate method for the preparation of N-methyl-N-(3,4-dichlorostyryl)acetamidine involves the N-methylation of N-(3,4-dichlorostyryl)acetamidine (9.2 g., 0.04 mole) with methyl fluorosulfonate (5.7 g., 0.05 mole) in 50 ml. of dichloromethane. The reaction mixture is basified with 10% sodium hydroxide and the organic layer separated, dried, and concentrated to provide the free base which is taken up in acetone and acidified with ethanolic hydrogen chloride. The product thus obtained is crystallized from ethanol-isopropyl ether to afford analytically pure N-METHYL-N-(3,4-DICHLOROSTYRYL)ACETAMIDINE HYDROCHLORIDE, m.p. 238°-239° C., (dec.)(corr.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04130663 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-8953ae87a7b9464ba1991630d77edf84 |
| Source note | uspto-grants-1978_12 |