HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 568980Erstellt: 25. Oktober 2026
Dimethyl Sulfoxide → 2,2-Difluoro-5-methoxy-1-pentanal hydrate
https://huagongshe.com/reaction/568980
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | 2,2-Difluoro-5-methoxypentan-1-ol | HCID 14097599 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2,2-Difluoro-5-methoxy-1-pentanal hydrate | HCID 20149453 | 53,4% |
Reaktionsschritte
A solution of dry dimethylsulfoxide (3 g, 38 mmoles) in dry dichloromethane (15 ml) is slowly added to a solution of oxalyl chloride (2.4 g, 19 mmoles) in dichloromethane (15 ml), kept under nitrogen and cooled to -60° C. Stirring is continued for 15 min. at -60° C. and followed by addition of 2,2-difluoro-1-hydroxy-5-methoxypentane (2.7 g, 17.5 mmoles) in dichloromethane (15 ml). The reaction mixture is stirred for 11/2 hours at -60° C., triethylamine (8.4 ml, 114 mmoles) in dichloromethane (15 ml) is slowly added, and the cooling bath is removed. The reaction mixture is hydrolyzed with brine and diluted with dichloromethane. The organic phase is then washed successively with 2N HCl containing some sodium chloride, and brine. Usual work-up affords the title compound (1.59 g, 53%) which is used for the next step without further purification.
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-7857d77b235a47458505ec6d65fe4927 |
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| Quellennotiz | uspto-grants-1988_03 |
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