HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 19354077, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Sodium Bromide | HCID 253881 | — |
| Reactant | methyloctadecylsulfide | HCID 536381 | — |
| Reactant | Sodium hexafluoroantimonate | HCID 16689647 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 19354077 | HCID 19354077 | — |
Reaction Steps
In a 100 mL Erlenmeyer flask were combined 10 g (0.05 mol) phenacyl bromide, 12.93 g (0.05 mol) sodium hexafluoroantimonate, 15 g (0.05 mol) methyl octadecyl sulfide and 40 mL methyl ethyl ketone (2-butanone). The reaction mixture was heated to boiling and maintained at this temperature for 30 minutes. During this time, sodium bromide was observed to precipitate. The reaction mixture was filtered to remove the inorganic salts and the resulting solution placed on a rotary evaporator to remove solvents. The product crystallized to give the desired salt, m.p. 80-82° C. Recrystallization from isopropanol gave a very light tan salt with a melting point of 79-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06031014 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-4e7a78235a094b98b9fdb25f1cc51634 |
| Source note | uspto-grants-2000_02 |