Reaktion #1350560

ord-9bde9e01a4bf40ad94a7370e311e8468

Reaktionsgleichung

[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
Ausbeute 32.5%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  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
    Sonstigeonto crushed ice slurry (200 g)
  5. 5
    Sonstigethe resulting precipitate was collected
  6. 6
    Waschenwashed with cold water three times
  7. 7
    Sonstigeair-dried

Vorschrift

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+).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06540793B1uspto-grants-2003_04