Reaction #1702075

ord-bea219235cc346bca6eb4e273a38fed3

Reaction equation

[BH4-].[Na+]
sodium borohydride
COc1ccc(Br)c(C=O)c1
2-bromo-5-methoxybenzaldehyde
NC1CC1
cyclopropylamine
Cc1ccccc1
toluene
COc1ccc(Br)c(CNC2CC2)c1
crude product
COc1ccc(Br)c(CNC2CC2)c1
N-(2-bromo-5-methoxybenzyl)cyclopropanamine

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherIn a flask fitted with a Dean-Stark trap
  2. 2
    Temperatureat reflux for 4 hours
  3. 3
    ConcentrationThe solution was then concentrated
  4. 4
    Otherto give a yellow oil to which
  5. 5
    TemperatureThe reaction mixture was cooled on icebath
  6. 6
    workup.ADDITIONAfter complete addition
  7. 7
    workup.STIRRINGthe reaction mixture was stirred 2 hours at room temperature

Procedure

In a flask fitted with a Dean-Stark trap was introduced 2-bromo-5-methoxybenzaldehyde (5.68 g, 26.41 mmol), cyclopropylamine (3.02 g, 52.83 mmol) and toluene (70 ml). The reaction mixture was stirred at room temperature for 1 hour and then at reflux for 4 hours. The solution was then concentrated to give a yellow oil to which was added methanol (30 ml). The reaction mixture was cooled on icebath followed by portionwise addition of sodium borohydride (2.00 g, 52.83 mmol). After complete addition, the reaction mixture was stirred 2 hours at room temperature, and then water (70 ml) was added. The crude product was isolated by extraction with dichloromethane and the combined organic phases were dried over sodium sulfate, filtered, and finally evaporated under reduced pressure.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08765728B2uspto-grants-2014_07