HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Bromoethyl)naphthalene → 4,6-Diamino-1,2-dihydro-2,2-dimethyl-1-[2-(naphth-1-yl)ethoxy]-1,3,5-triazine hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Bromoethyl)naphthalene | HCID 139541 | — |
| Reactant | 4,6-Diamino-1,2-dihydro-1-hydroxy-2,2-dimethyl-1,3,5-triazine | HCID 19089922 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4,6-Diamino-1,2-dihydro-2,2-dimethyl-1-[2-(naphth-1-yl)ethoxy]-1,3,5-triazine hydrobromide | HCID 19089946 | 20.4% |
Reaction Steps
This compound was prepared in a manner analogous to that of Example 3, Step F, using 0.8 gram (0.005 mole) of 4,6-diamino-1,2-dihydro-1-hydroxy-2,2-dimethyl-1,3,5-triazine (prepared in Example 3) and 1.3 grams (0.006 mole) of 2-(naphth-1-yl)ethyl bromide (commercially available) in 15 ml of dimethylformamide. The reaction product was recrystallized from water, yielding 0.4 gram of 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-[2-(naphth-1-yl)ethoxy]-1,3,5-triazine hydrobromide. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05300503 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-f6b1f6c2e4574b6999a1c1ca9d3208b9 |
| Source note | uspto-grants-1994_04 |