HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 20443108, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | (5-Chloro-2,1,3-benzothiadiazol-4-yl)cyanamide | HCID 13785516 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20443108 | HCID 20443108 | — |
Reaction Steps
The starting material is obtained as follows: 5 g 5-chloro-N-cyano-2,1,3-benzothiadiazol-4-amine are added to a solution of 0.55 g sodium in 60 ml ethanol and the mixture is reacted with 3 g allyl bromide. The mixture is agitated 3 hours under refluxing and the solvent evaporated under vacuum. The residue is extracted with methylene chloride. N-allyl-5-chloro-N-cyano-2,1,3-benzothiadiazol-4-amine (M.P. 62°-63°) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04476135 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-a93c9c0d514d4bd39fa8e8327b010cca |
| Source note | uspto-grants-1984_10 |