HuagongsheHuagongshe Chemistry Print Report · For research reference only
Crotononitrile → Evandamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Crotononitrile | HCID 637921 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 23312423 | HCID 23312423 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Evandamine | HCID 3038554 | 60.9% |
Reaction Steps
20 g of 2-hydrazino-4,5,6,7-tetrahyro-benzothiazole hydrochloride are added to a sodium ethylate solution of 5.7 g of sodium and 250 ml of ethanol and the mixture is stirred at room temperature for 10 minutes. 5.5 g of crotononitrile are then added dropwise and the mixture is boiled under reflux for 5 hours. After cooling, the ethanol is stripped off in vacuo and the residue is taken up in water. The insoluble material is filtered off and washed thoroughly with water, acetone and ether in succession. After drying, 11.8 g of beige crystals of 3-amino-5-methyl-1-(4,5,6,7-tetrahydro-benzothiazolyl)-2-pyrazoline of melting point 247°-249° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04600722 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-49c689f31b734893be0dda0216d25fa6 |
| Source note | uspto-grants-1986_07 |