HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Azobisisobutyronitrile → 6-Bromomethyl-nicotinic acid methyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Azobisisobutyronitrile | HCID 6547 | — |
| Edukt | Hexane | HCID 8058 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | Methyl 6-methylnicotinate | HCID 231548 | — |
| Lösungsmittel | Carbon Tetrachloride | HCID 5943 | — |
| Produkt | 6-Bromomethyl-nicotinic acid methyl ester | HCID 12752237 | 35,5% |
Reaktionsschritte
To a solution of methyl 6-methylnicotinate (6.3 g) in carbon tetrachloride (100 mL) is added successively N-bromosuccinimide (8.9 g) and 2,2′-azobisisobutyronitrile (342 mg), and the mixture is refluxed under heating for 6 hours. After cooling to room temperature, to the reaction mixture is added n-hexane (300 mL) and the insoluble materials are removed by filtration. The filtrate is concentrated in vacuo and the resultant crude product is purified by column chromatography on silica gel (Solvent; n-hexane:ethyl acetate=10:1) and stirred in n-hexane to give methyl 6-(bromomethyl)nicotinate (3.4 g, yield; 35%) as colorless crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07384952B2 |
| Quelldatensatz | uspto-grants-2008_06 |
| ORD ID | ord-88834c4755c14761a72f39e7f625bef1 |
| Quellennotiz | uspto-grants-2008_06 |