Reacción #1350560

ord-9bde9e01a4bf40ad94a7370e311e8468

Ecuación de reacción

[BH4-].[Na+]
sodium borohydride
Cc1ccc(N)cc1O
5-amino-2-methylphenol
O=Cc1cccs1
2-thiophenecarboxaldehyde
CC(=O)[O-].[Na+]
sodium acetate
Cc1ccc(N(C)c2cccs2)cc1O
2-methyl-5-(thiophen-2-yl-methylamino)phenol
Rendimiento 32.5%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  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
    Otroonto crushed ice slurry (200 g)
  5. 5
    Otrothe resulting precipitate was collected
  6. 6
    Lavadowashed with cold water three times
  7. 7
    Otroair-dried

Procedimiento

To a solution of 5-amino-2-methylphenol (12.30 g, 100 mmole) in methanol (100 mL) at 4° C. was added 2-thiophenecarboxaldehyde (16.82 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-(thiophen-2-yl-methylamino)phenol (7.12 g, 32% yield): mp 130.8-132.6° C.; 1HNMR (400 MHz, DMSO-d6) δ 1.94 (s, 3H), 4.34 (d, 2H, J=6.0 Hz), 5.91 (t, 1H, J=6.1 Hz), 6.00 (dd, 1H, J=2.3, 8.0 Hz), 6.11 (d, 1H, J=2.2 Hz), 6.70 (d, 1H, J=8.1 Hz), 6.95 (dd, 1H, J=3.5, 5.0 Hz), 7.00 (dd, 1H, J=0.8, 3.4 Hz), 7.34 (dd, 1H, J=1.0, 5.0 Hz), 8.79 (s, 1H); MS m/z 219 (M+).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06540793B1uspto-grants-2003_04