Boron trifluoride etherate → HCID 84732417, Verbindung
Reaktionsgleichung
C([SiH](CC)CC)C.B(F)(F)F.CCOCC.[Cl:17][C:18]1[CH:19]=[C:20]2[C:24](=[CH:25][CH:26]=1)[C:23](=[O:27])[NH:22][C:21]2(O)[CH3:28].[Cl:30][C:31]1[CH:39]=[C:38]2[C:34]([C:35](O)([CH3:41])[NH:36][C:37]2=[O:40])=[CH:33][CH:32]=1.C([O-])(O)=O.[Na+]>C(Cl)Cl>[Cl:17][C:18]1[CH:19]=[C:20]2[C:24](=[CH:25][CH:26]=1)[C:23](=[O:27])[NH:22][CH:21]2[CH3:28].[Cl:30][C:31]1[CH:39]=[C:38]2[C:34]([CH:35]([CH3:41])[NH:36][C:37]2=[O:40])=[CH:33][CH:32]=1Komponenten
Edukt 5
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Under N2 protection, triethylsilane (23 g, 200 mmol) and trifluoroboron etherate (8.51 g, 60 mmol) were added successively at −15° C. to a mixture of 5-chloro-3-hydroxy-3-methyl-2,3-dihydro-isoindol-1-one and 6-chloro-3-hydroxy-3-methyl-2,3-dihydro-isoindol-1-one (3.95 g, 20 mmol) in dry DCM (100 mL). Afterwards, the reaction mixture was stirred at room temperature for 2 hours and a saturated aqueous solution of NaHCO3 (30 mL) was added. The mixture was then extracted with DCM and the organic layer was washed with brine, dried over anhy. Na2SO4, filtered and concentrated in vacuo to give a crude mixture of products. The two regioisomers were separated by prep-HPLC to give the title compounds, 5-chloro-3-methyl-2,3-dihydro-isoindol-1-one (0.4 g, 11%) and 6-chloro-3-methyl-2,3-dihydro-isoindol-1-one (0.35 g, 9.6%) as white solids. MS: 182.0 (M+H+).
Aufarbeitung
- extractionThe mixture was then extracted with DCM
- washthe organic layer was washed with brine
- customdried over anhy
- filtrationNa2SO4, filtered
- concentrationconcentrated in vacuo
- customto give a crude
- additionmixture of products
- customThe two regioisomers were separated by prep-HPLC
Quellen und Nachweise
- ORD-Eintrag
- ord-88c7f1e9b6ae42a2923650cd45745ea9
- Quelldatensatz
- uspto-grants-2015_09
- Patentnummer
- US09133158B2
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