Methyl 4-Formylbenzoate → 4-[(4-Cyclohexylphenylimino)methyl]benzoic acid methyl ester

HRID 967626Notes

Reaction equation

HRID 967626 reaction equation
[CH3:1][O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][C:7]([CH:10]=O)=[CH:6][CH:5]=1.[CH:13]1([C:19]2[CH:25]=[CH:24][C:22]([NH2:23])=[CH:21][CH:20]=2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1>CO>[CH3:1][O:2][C:3](=[O:12])[C:4]1[CH:9]=[CH:8][C:7]([CH:10]=[N:23][C:22]2[CH:24]=[CH:25][C:19]([CH:13]3[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]3)=[CH:20][CH:21]=2)=[CH:6][CH:5]=1

Participants

4

Conditions

Temperature
0 °C

Procedure

4-Formylbenzoic acid methyl ester (6.65 g, 40.5 mmol) was dissolved in hot methanol (175 mL). To this mixture, 4-cyclohexylaniline (7.1 g, 40.5 mmol) was added. To the resulting suspension, more methanol (75 mL) was added and the mixture was heated at reflux for 1 hour. After cooling to 0° C., the mixture was filtered and the solid was washed with ice-cold methanol and dried in vacuo at 40° C. for 16 hours to afford 10.95 g of 4-[(4-cyclohexylphenylimino)-methyl]benzoic acid methyl ester. This compound (10.93 g, 34 mmol) was suspended in methanol (200 mL) and glacial acetate acid (27 mL) was added followed by sodium cyano borohydride (1.9 g, 30 mmol) in small portions. The mixture was stirred at room temperature for 1 hour and concentrated in vacuo. The residue was dissolved in DCM (200 mL) and washed with 5% aqueous sodium carbonate (5×80 mL), dried (magnesium sulphate) and concentrated in vacuo. The residue was added ethyl acetate (100 mL) and n-heptane (200 mL) and concentrated in vacuo to half the original volume. The solid was filtered, washed with n-heptane and dried in vacuo at 40° C. for 16 hours to afford 9.52 g (87%) of 4-((4-cyclohexylphenylamino)methyl)benzoic acid methyl ester.

Workup

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 1 hour
  3. filtrationthe mixture was filtered
  4. washthe solid was washed with ice-cold methanol
  5. customdried in vacuo at 40° C. for 16 hours

Sources & evidence

ORD record
ord-4d5ac7d71bc34307adc008c794aee543
Source dataset
uspto-grants-2005_10
Patent number
US06953812B2

Reaction notes

Loading…