HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 568982Erstellt: 25. Oktober 2026
2-Dimethylaminopyridine → 2,2-Difluoro-5-methoxyvaleronitrile
https://huagongshe.com/reaction/568982
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Dimethylaminopyridine | HCID 21885 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 2-Amino-3,4-dimethylpyridine | HCID 11007884 | — |
| Edukt | 2,2-Difluoro-5-methoxy-1-pentanal oxime | HCID 73664053 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2,2-Difluoro-5-methoxyvaleronitrile | HCID 14097600 | 67,1% |
Reaktionsschritte
Thionyl chloride (809 mg, 6.8 mmoles) in ice cold dry dichloromethane (7 ml) is added to a solution of dimethylamino pyridine (903 mg, 7.4 mmoles) in dichloromethane (15 ml) kept under nitrogen and cooled at -15° C. The oxime 34 (1.04 g, 6.2 mmoles), dissolved in dichloromethane (20 ml) is added, followed by addition of dimethyl aminopyridine as a solid (903 mg, 7.4 mmoles). The reaction mixture is then allowed to rise to room temperature, kept at 25° C. for 1 hour, diluted with dichloromethane, washed with 1N HCl, and finally with water. Concentration of the organic phase, previously dried over sodium sulfate, (30° C., 100 mm Hg) affords the title compound (620 mg) which is purified by bulb to bulb distillation (50° C., 30 mm Hg): 485 mg (52%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04730006 |
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| Quelldatensatz | uspto-grants-1988_03 |
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| ORD ID | ord-9af99a4085184e959ef37b2a1fab5840 |
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| Quellennotiz | uspto-grants-1988_03 |
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