HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 21107328, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 21107316 | HCID 21107316 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21107328 | HCID 21107328 | 93.4% |
Reaction Steps
To a suspension of sodium hydride (60%, 0.7 g, 16.8 mmol) in anhydrous N,N-dimethylformamide (80 ml) was added 5-allyl-quinolin-6-ol (intermediate 5) (2.68 g, 14 mmol) slowly at room temperature. The reaction mixture was stirred for 1 hour, then benzyl bromide (2.57 ml, 21 mmol) was added. The mixture was allowed to stir for 1.5 hrs at room temperature, quenched with water and extracted with methylene chloride. The organic layer was washed with water, dried over anhydrous sodium sulfate and filtered. The solvent was removed under vacuum. Chromatography (30% hexanes-ethyl acetate) afforded 3.6 g (92%) of 5-allyl-6-benzyloxy-quinoline as a light brown oil. MS ESI m/z 276 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07227023B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-bb4c30f5ce0c4853956763fcced2dee6 |
| Source note | uspto-grants-2007_06 |