Sulfuric Acid → 1h-Benzimidazole-2-propanoic acid, ethyl ester

HRID 507266Notes

Reaction equation

HRID 507266 reaction equation
[C:1]1([NH2:8])[C:2]([NH2:7])=[CH:3][CH:4]=[CH:5][CH:6]=1.[C:9]1(=O)OC(=O)C[CH2:10]1.S(=O)(=O)(O)[OH:17].O1[CH2:26][CH2:25][O:24][CH2:23][CH2:22]1>C(O)C>[NH:7]1[C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][C:1]=2[N:8]=[C:9]1[CH2:10][CH2:22][C:23]([O:24][CH2:25][CH3:26])=[O:17]

Participants

6

Conditions

Temperature
80 °C

Procedure

To a stirred solution of benzene-1,2-diamine (20.0 g, 0.19 mol, 1.0 eq.) in dioxane (500 mL) at room temperature, was added succinic anhydride (22.2 g, 0.22 mol, 1.2 eq.), and the reaction mixture was heated to 80° C. and stirred at that temperature for 16 hours. The resulting precipitate was filtered and washed with dioxane (100 mL), water (100 mL) and diethyl ether (100 mL) to give a white solid. The solid was suspended in ethanol (400 mL), and concentrated sulfuric acid (10 mL) was added at room temperature. The reaction mixture was heated to reflux and stirred at that temperature for 20 hours. The reaction was then cooled to room temperature and concentrated in vacuo. Water (100 mL) was added, and the mixture was adjusted to pH 7 with 1 M aqueous NaOH solution. The aqueous layer was extracted into ethyl acetate (3×100 mL), and the combined organic extracts were dried over magnesium sulfate and concentrated in vacuo to give 6a as a pale-orange oil (15.6 g, 46%).

Workup

  1. filtrationThe resulting precipitate was filtered
  2. washwashed with dioxane (100 mL), water (100 mL) and diethyl ether (100 mL)
  3. customto give a white solid
  4. temperatureThe reaction mixture was heated
  5. temperatureto reflux
  6. stirringstirred at that temperature for 20 hours
  7. temperatureThe reaction was then cooled to room temperature
  8. concentrationconcentrated in vacuo
  9. additionWater (100 mL) was added
  10. extractionThe aqueous layer was extracted into ethyl acetate (3×100 mL)
  11. dry with materialthe combined organic extracts were dried over magnesium sulfate
  12. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-781e1f4fe97948a7add7c15923ca564b
Source dataset
uspto-grants-2010_08
Patent number
US07786139B2

Reaction notes

Loading…