HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 56626424, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | HCID 178448763 | HCID 178448763 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 56626424 | HCID 56626424 | 40% |
Reaction Steps
26.6 g (0.22 mol) of allyl bromide were added to a solution of 43.6 g (0.2 mol) of 4-amino-6-fluoro-tert.-butyl-3-mercapto-1,2,4-triazin-5-one in 200 ml of 1 N sodium hydroxide solution at room temperature. The reaction mixture was stirred for approximately 20 hours at room temperature, the organic phase was then taken up in chloroform, and the solution was washed with three times 150 ml of 0.1 N sodium hydroxide solution, dried over sodium sulphate, filtered and concentrated. The oily residue was degassed at 50° C./0.05 mbar, and recrystallized from ethyl acetate/petroleum ether. 20.8 g (40% of theory) of 3-allylthio-4-amino-6-fluoro-tert.-butyl-1,2,4-triazin-5-one of melting point 75° to 74° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04470842 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-a65f8d25abe948d0b908879ad2187c82 |
| Source note | uspto-grants-1984_09 |