Dimethylformamide → 5-Fluoro-1,3-benzothiazole-2-carbaldehyde
Reaktionsgleichung
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][CH:8]=[N:7][C:6]=2[CH:10]=1.C([Li])CCC.CN(C)[CH:18]=[O:19]>C(OCC)C.CCCCCC>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][C:8]([CH:18]=[O:19])=[N:7][C:6]=2[CH:10]=1Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- -50 °C
Versuchsvorschrift
To a stirred solution of 36 g of 5-fluorobenzothiazole in 100 ml of diethyl ether cooled to -70° C. was added dropwise over a 5 minute period 9.4 ml of a 2.5M solution of n-butyl lithium in hexane. The reaction mixture was allowed to warm to -50° C. for one hour and was then cooled to -78° C. Dry dimethylformamide (2.8 ml) was added dropwise and the reaction mixture allowed to warm to room temperature over a period of two hours. The reaction was diluted with 300 ml of diethyl ether and washed with 1N hydrochloric acid (1×40 ml), water (1×40 ml), a saturated sodium bicarbonate solution (1×40 ml) and dried over magnesium sulfate. The solvent was removed and the residual product flash chromatographed on silica (50% ethyl acetate--hexane; v:v) to give 24.7 g of the titled product, m.p. 105°-107° C.
Aufarbeitung
- temperaturewas then cooled to -78° C
- temperatureto warm to room temperature over a period of two hours
- washwashed with 1N hydrochloric acid (1×40 ml), water (1×40 ml)
- dry with materiala saturated sodium bicarbonate solution (1×40 ml) and dried over magnesium sulfate
- customThe solvent was removed
- customthe residual product flash chromatographed on silica (50% ethyl acetate--hexane; v:v)
Quellen und Nachweise
- ORD-Eintrag
- ord-3e850f0d73d644b18e9a1342a678da7a
- Quelldatensatz
- uspto-grants-1994_06
- Patentnummer
- US05322847
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