Hydrochloric Acid → 2-Benzyl-4-methyl-isoindole-1,3-dione

HRID 2427640Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2427640
[CH2:1]([NH2:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:9][C:10]1[CH:18]=[CH:17][CH:16]=[C:15]2[C:11]=1[C:12](=[O:20])[O:13][C:14]2=O.C[Si](N[Si](C)(C)C)(C)C.Cl>C1C=CC=CC=1.[I-].[Zn+2].[I-]>[CH2:1]([N:8]1[C:12](=[O:20])[C:11]2[C:15](=[CH:16][CH:17]=[CH:18][C:10]=2[CH3:9])[C:14]1=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

7

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A solution of benzylamine (0.655 mL, 6 mmol) in benzene (5 mL) was added to a stirred solution of 4-methyl-isobenzofuran-1,3-dione (0.81 g, 5 mmol) in dry benzene (20 mL). An exothermic reaction was observed during this addition. The resulting solution was stirred for an additional 1 h. After this time, zinc iodide (1.92 g, 6 mmol) was added in one portion and the resulting mixture heated to 80° C. To this suspension HMDS (1.48 mL, 7 mmol) in benzene (10 mL) was added slowly and stirred at 80° C. for 1 h. The reaction mixture was cooled to room temperature and treated with 0.5 N HCl (15 mL). The organic phase was separated and the aqueous was extracted with ethyl acetate (2×25 mL). The combined organic extracts were washed with aqueous NaHCO3 (10 mL), dried over MgSO4, filtered and concentrated to afford 2-benzyl-4-methyl-isoindole-1,3-dione (1 g, 80%). 1H NMR (300 MHz, CDCl3): δ (ppm) 2.69 (s, 3H), 4.83 (s, 2H), 7.26-7.59 (m, 7H), 7.67 (d, 1H).

Aufarbeitung

  1. customAn exothermic reaction
  2. additionwas observed during this addition
  3. stirringstirred at 80° C. for 1 h
  4. temperatureThe reaction mixture was cooled to room temperature
  5. customThe organic phase was separated
  6. extractionthe aqueous was extracted with ethyl acetate (2×25 mL)
  7. washThe combined organic extracts were washed with aqueous NaHCO3 (10 mL)
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-9fb47f62029c4c08b83e811bef5221e6
Quelldatensatz
uspto-grants-2011_06
Patentnummer
US07968570B2

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