Dichloromethane → Benzyl 3-formyl-2-methylphenylcarbamate

HRID 2361269Notes

Reaction equation

HRID 2361269 reaction equation
[C:1]([C:3]1[C:4]([CH3:20])=[C:5]([NH:9][C:10](=[O:19])[O:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:6]=[CH:7][CH:8]=1)#N.CC(C[AlH]CC(C)C)C.ClCCl.[O:33]1CCCC1>>[CH:1]([C:3]1[C:4]([CH3:20])=[C:5]([NH:9][C:10](=[O:19])[O:11][CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:6]=[CH:7][CH:8]=1)=[O:33]

Participants

5

Conditions

Temperature
-78 °C

Procedure

To a solution of benzyl 3-cyano-2-methylphenylcarbamate (6.41 g, 24.07 mmol) in tetrahydrofuran (250 mL) at −78° C. was added DIBAL-H in dichloromethane (96 mL, 96 mmol) over 1 hr. The mixture was stirred at −78° C. for 45 min and then at room temperature for 5 hr. It was poured into ice cold water (300 mL) and the resulting mixture was stirred at room temperature for 30 min. The mixture was filtered through CELITE®, and the filtrate was concentrated to remove most of the THF. The remaining aqueous solution was extracted with ethyl acetate (4×150 mL). The combined extract was dried over anhydrous MgSO4. Removal of solvent under vacuum provided the desired product (5.65 g, 20.98 mmol, 87% yield) as a pale yellow solid.

Workup

  1. waitat room temperature for 5 hr
  2. stirringthe resulting mixture was stirred at room temperature for 30 min
  3. filtrationThe mixture was filtered through CELITE®
  4. concentrationthe filtrate was concentrated
  5. customto remove most of the THF
  6. extractionThe remaining aqueous solution was extracted with ethyl acetate (4×150 mL)
  7. extractionThe combined extract
  8. dry with materialwas dried over anhydrous MgSO4
  9. customRemoval of solvent under vacuum

Sources & evidence

ORD record
ord-a9e365cb8c874641a075706d32a7be74
Source dataset
uspto-grants-2014_04
Patent number
US08685969B2

Reaction notes

Loading…