Sulfuric Acid → 6-Methoxy-3-(trichloromethyl)-2-benzofuran-1(3H)-one
Reaktionsgleichung
[Cl-].[Cl-].[Ca+2].[CH3:4][O:5][C:6]1[CH:7]=[C:8]([CH:12]=[CH:13][CH:14]=1)[C:9]([OH:11])=[O:10].[Cl:15][C:16]([Cl:21])([Cl:20])[CH:17](O)O.OS(O)(=O)=O>>[CH3:4][O:5][C:6]1[CH:7]=[C:8]2[C:12]([CH:17]([C:16]([Cl:21])([Cl:20])[Cl:15])[O:10][C:9]2=[O:11])=[CH:13][CH:14]=1Komponenten
Versuchsvorschrift
A oven-dried 25 mL three neck round-bottomed flask containing a stirring bar was fitted with a drying tube (CaCl2) and was charged with m-methoxybenzoic acid (5.04 g, 17.91 mmol) followed by chloral hydrate (2.96 g, 17.91 mmol). Concentrated H2SO4 (12.0 mL) was added and the reaction mixture was left stirring at room temperature for 24 h. It was then poured onto ice, a thick precipitate formed and the mixture was left stirring vigorously until the ice was dissolved. The precipitate was filtered, washed with water and dried. The solid was recrystallised from ethanol, the crystals were then filtered and dried to yield 6-methoxy-3-(trichloromethyl)isobenzofuran-1(3H)-one as off-white needles (3.16 g, 63%). Spectral data for this compound were consistent with those in the literature. M.p. 134-136° C. (lit. m.p. 136-137° C.); 1H NMR (400 MHz, DMSO-d6): δ=7.88 (d, J=8.3 Hz, 1H), 7.49-7.39 (m, 2H), 6.54 (s, 1H), 3.90 (s, 3H).
Aufarbeitung
- waitthe reaction mixture was left
- additionIt was then poured onto ice
- customa thick precipitate formed
- waitthe mixture was left
- dissolutionwas dissolved
- filtrationThe precipitate was filtered
- washwashed with water
- customdried
- customThe solid was recrystallised from ethanol
- filtrationthe crystals were then filtered
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-53c37fe24b6a4849b58cc420e9a8bac6
- Quelldatensatz
- uspto-grants-2015_06
- Patentnummer
- US09050586B2
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