Water → 4-Phthalimidobutyronitrile

HRID 23145Notes

Reaction equation

HRID 23145 reaction equation
[C:1]1(=[O:11])[NH:5][C:4](=[O:6])[C:3]2=[CH:7][CH:8]=[CH:9][CH:10]=[C:2]12.[K].O>CN(C=O)C>[C:4]([CH2:3][CH2:2][CH2:1][N:5]1[C:1](=[O:11])[C:2]2=[CH:10][CH:9]=[CH:8][CH:7]=[C:3]2[C:4]1=[O:6])#[N:5]

Participants

4

Conditions

Temperature
90 °C

Procedure

A mixture of potassium phthalimide (8.48 g, 0.046 mol) and 4-bromopropylcyanide (6.4 g, 0.043 mol) in 50 ml of anhydrous DMF was stirred at 90° C. for 2 h. After dilution with 300 ml of water, the aqueous solution was extracted with chloroform (80 ml×3). The combined chloroform solution was washed with 0.5% NaOH aqueous solution (80 ml) and water (100 ml), and dried over anhydrous Na2SO4. After evaporation of chloroform, an oil was obtained and 300 ml of water was added. The oil was rapidly solidified. The solid formed was collected by filtration, washed with water, and dried under high vacuum. The product was recrystallized from methanol which was diluted with water, to give white crystals (7.75 g, 84%). 1H NMR (CDCl3) δ7.87 (dd, 2H), 7.75 (dd, 2H), 3.83 (t, 2H), 2.44 (t, 2H), 2.09 (quintet, 2H).

Workup

  1. extractionAfter dilution with 300 ml of water, the aqueous solution was extracted with chloroform (80 ml×3)
  2. washThe combined chloroform solution was washed with 0.5% NaOH aqueous solution (80 ml) and water (100 ml)
  3. dry with materialdried over anhydrous Na2SO4
  4. customAfter evaporation of chloroform
  5. customan oil was obtained
  6. customThe solid formed
  7. filtrationwas collected by filtration
  8. washwashed with water
  9. customdried under high vacuum
  10. customThe product was recrystallized from methanol which
  11. additionwas diluted with water

Sources & evidence

ORD record
ord-d989185980c245c7bc26ebeea978d823
Source dataset
uspto-grants-2005_02
Patent number
US06849713B2

Reaction notes

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