반응 #1702075

ord-bea219235cc346bca6eb4e273a38fed3

반응 방정식

[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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타In a flask fitted with a Dean-Stark trap
  2. 2
    온도at reflux for 4 hours
  3. 3
    농축The solution was then concentrated
  4. 4
    기타to give a yellow oil to which
  5. 5
    온도The 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

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08765728B2uspto-grants-2014_07