HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 416615, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178527775 | HCID 178527775 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 416615 | HCID 416615 | 83.1% |
Reaction Steps
To a suspension of 2-Mercaptobenzimidazole (0.06M, 9 g) in methanol (50 ml) was added sodium hydroxide (0.06M, 2.4 g) and stirred for 30 min. to get a clear solution. To this solution, phenacyl bromide (0.05M, 10 g) was added slowly and stirred until the solid separates. The solid was filtered and washed thoroughly with 5% sodium hydroxide solution and methanol to get white solid (11.2 g). M.P. 167° C. NMR (DMSO): δ5.1(s, 2H, CH2), 7-8.2(m, 10H, Aromatic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06919389B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-1e353d21e435465783d9265deb5f1495 |
| Source note | uspto-grants-2005_07 |