HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 58171030, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 4-Bromo-5,6-dimethylpyridin-2-ol | HCID 46916251 | — |
| Catalyst | HCID 178418647 | HCID 178418647 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 58171030 | HCID 58171030 | — |
Reaction Steps
4-Bromo-5,6-dimethyl-2(1H)-pyridinone (1 eq.), prepared according to the procedure described by McElroy, W. T.; DeShong, P. Organic Letters 2003, 5, 4779-4782, was suspended in benzene (0.13 M). To this was then added silver carbonate (0.6 eq.) and benzyl bromide (1.2 eq.) before the suspension was heated at 45° C. for 3 days in the dark. The reaction suspension was cooled to RT, diluted with benzene and filtered through a bed of celite. The filtrate was washed with sat. aq. NaHCO3, dried over Na2SO4, filtered and the filtrate concentrated in vacuo. Purification by way of column chromatography (SiO2, Hex→10:1 (v/v) Hex:EtOAc) afforded the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889714B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-0d4e7709a85d4158bd42dc103fcc5e71 |
| Source note | uspto-grants-2014_11 |