Dimethyl Sulfoxide → 1,3-Dihydro-1,3-dioxo-2H-isoindole-2-butanal

Temperatur

-78 °C

To a 250-mL round-bottom flask, purged and maintained with an inert atmosphere of nitrogen, was added a solution of oxalic dichloride (2.52 g, 19.85 mmol, 1.98 equiv) in 40 mL of anhydrous dichloromethane. This solution was cooled to −78° C. under nitrogen. A solution of DMSO (1.56 g, 19.97 mmol, 1.99 equiv) in dichloromethane (10 mL) was added dropwise with stirring at −78° C. and the resulting solution was stirred for 20 min at −78° C. A solution of 2-(4-hydroxybutyl)-2,3-dihydro-1H-isoindole-1,3-dione (2.2 g, 10.03 mmol, 1.00 equiv) in 20 mL of dichloromethane was added dropwise with stirring. Stirring was continued for 20 min at −78° C., and then TEA (8.1 g, 80.20 mmol, 7.99 equiv) was added via syringe at the same temperature. The resulting solution was allowed to react, with stirring, for an additional 60 min at 0° C. After completion, the resulting mixture was diluted with 1 M aqueous hydrochloric acid, extracted with DCM, washed with 3×100 mL of brine, dried over sodium sulfate and concentrated under vacuum. The residue was purified by a silica gel column with ethyl acetate/petroleum ether (1:1) to provide the desired 4-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)butanal (1.9 g, 87%) as a white solid. MS (ES): m/z 218 (M+H)+.

1. customTo a 250-mL round-bottom flask, purged
2. temperaturemaintained with an inert atmosphere of nitrogen
3. stirringthe resulting solution was stirred for 20 min at −78° C
4. stirringwith stirring
5. stirringStirring
6. customto react
7. stirringwith stirring, for an additional 60 min at 0° C
8. extractionextracted with DCM
9. washwashed with 3×100 mL of brine
10. dry with materialdried over sodium sulfate
11. concentrationconcentrated under vacuum
12. customThe residue was purified by a silica gel column with ethyl acetate/petroleum ether (1:1)

ORD-Eintrag

ord-46da0adbaa5443e3afe151eb8f2d9a22

Quelldatensatz

uspto-grants-2015_12

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US09212190B2