Réaction #1350559

ord-a71e006aeb984d1b85777373029e8dc1

Équation de réaction

[BH4-].[Na+]
sodium borohydride
Cc1ccc(N)cc1O
5-amino-2-methylphenol
O=Cc1ccco1
2-furaldehyde
CC(=O)[O-].[Na+]
sodium acetate
Cc1ccc(N(C)c2ccco2)cc1O
2-methyl-5-(furan-2-yl-methylamino)phenol
Rendement 83.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    workup.STIRRINGto stir for an additional 1.5 hours
  3. 3
    workup.ADDITIONThe reaction mixture was poured
  4. 4
    Autreonto crushed ice slurry (200 g)
  5. 5
    Autrethe resulting precipitate was collected
  6. 6
    Lavagewashed with cold water three times
  7. 7
    Autreair-dried

Mode opératoire

To a stirred solution of 5-amino-2-methylphenol (12.30 g, 100 mmole) in methanol (100 mL) at 4° C. was added 2-furaldehyde (14.41 g, 150 mmole) and sodium acetate (16.41 g, 200 mmole). The reaction mixture was stirred for 15 minutes and sodium borohydride (4.73 g, 125 mmole) was added portionwise over 1 hour at 4° C. After the addition was complete, the reaction was allowed to stir for an additional 1.5 hours. The reaction mixture was poured onto crushed ice slurry (200 g) and the resulting precipitate was collected, washed with cold water three times and air-dried to afford 2-methyl-5-(furan-2-yl-methylamino)phenol (16.86 g, 83% yield): mp 126.8-128.5° C.; 1HNMR (400 MHz, DMSO-d6) δ 1.94 (s, 3H), 4.12 (d, 2H, J=6.1 Hz), 5.71 (t, 1H, J=6.1 Hz), 6.00 (dd, 1H, J=2.3, 8.0 Hz), 6.11 (d, 1H, J=2.2 Hz), 6.22 (d, 1H, J=3.0 Hz), 6.36 (m, 1H), 6.70 (d, 1H, J=8.1 Hz), 7.54 (t, 1H, J=0.8 Hz), 8.79 (s, 1H); MS m/z 203 (M+).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06540793B1uspto-grants-2003_04