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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1526604Erstellt: 27. Oktober 2026

Acetonitrile, difluoro- → Methyl 2-(difluoromethyl)-4,5-dihydrooxazole-4-carboxylate

https://huagongshe.com/reaction/1526604

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrile, difluoro-HCID 120219—
EduktMethyl DL-serinate hydrochlorideHCID 517373—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
ProduktMethyl 2-(difluoromethyl)-4,5-dihydrooxazole-4-carboxylateHCID 9038934889,1%

Reaktionsschritte

To a cooled (0° C.) solution of sodium methoxide (25 wt % solution in methanol; 0.230 mL, 1.032 mmol) and MeOH (20 mL) was added dropwise difluoroacetonitrile (0.690 mL, 10.03 mmol) while maintaining an internal temperature of <1° C. After 20 min DL-serine methyl ester hydrochloride (1.55 g, 9.96 mmol) was added followed by MeOH (20 mL) and the reaction was allowed to warm to rt overnight. Subsequently, the reaction was heated to 55° C. for 5 h. The reaction was cooled to rt and partitioned between DCM/water. The aqueous layer was extracted with DCM (3×) and the combined organic layers were washed with water and dried over MgSO4. The filtrate was concentrated in vacuo to give 1.59 g (89%) of a light-brown oil. MS m/z=180 [M+H]+. Calculated for C6H7F2NO3:179.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09085576B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-55f4bf2e098e4748920a2bc78e5442ee
Quellennotizuspto-grants-2015_07