HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl bromide → 4-Benzyloxy-1-butyl-1H-pyridin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Benzyloxy-2(1H)-pyridone | HCID 3607724 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Benzyloxy-1-butyl-1H-pyridin-2-one | HCID 59497072 | 98% |
Reaction Steps
1-Bromobutane (3.75 g, 27.33 mmol) and potassium carbonate (10.3 g, 74.52 mmol) were added to a solution of 4-benzyloxy-1H-pyridin-2-one (5.0 g, 24.84 mmol) in CH3CN (200 ml). The mixture was heated at reflux temperature for 16 h. The r.m. was then filtered through diatomaceous earth and concentrated in vacuo. The crude residue was then triturated with diethyl ether to yield pure D1 (6.26 g, 98%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08697689B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-b63a7ac91c2f4dee95ed745756e50781 |
| Source note | uspto-grants-2014_04 |