HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl bromide → HCID 13154052, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methyl-5-hydroxypyridine | HCID 14275 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 13154052 | HCID 13154052 | 48.4% |
Reaction Steps
A mixture of 11.0 g (0.10 mol) of 5-hydroxy-2-methylpyridine (commercially available), 13.8 g (0.10 mol) of n-butyl bromide and 6.00 g (0.04 mol) of anhydrous potassium carbonate with 100 ml of acetone was refluxed for 24 hours, the solvent was removed, 100 ml of water was added, and the mixture was extracted with chloroform. The chloroform layer was washed with water, dried over anhydrous sodium sulfate, and then concentrated under a reduced pressure. The residue was separated by silica gel column chromatography (ethyl acetate:hexane=1:4) to give 8.00 g of an oily product (yield 47.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05219847 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-9fcea58064e948168763654c286ba2e2 |
| Source note | uspto-grants-1993_06 |