반응 #2195481

ord-8c5b5efb94144665909875ba9b90ddc7

반응 방정식

N
ammonia
CNC.Cl
dimethylamine hydrochloride
CCCCC/C=C\C/C=C\CCCCCCCCOc1ccc(C=O)cc1OCCCCCCCC/C=C\C/C=C\CCCCC
3,4-dilinoleyloxybenzaldehyde
[BH4-].[Na+]
Sodium borohydride
CCCCC/C=C\C/C=C\CCCCCCCCOc1ccc(CN(C)C)cc1OCCCCCCCC/C=C\C/C=C\CCCCC
yellow oil
수율 74.4%
CCCCC/C=C\C/C=C\CCCCCCCCOc1ccc(CN(C)C)cc1OCCCCCCCC/C=C\C/C=C\CCCCC
N,N-Dimethyl-3,4-dilinoleyloxybenzylamine
수율 74.4%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGto stir at room temperature overnight
  2. 2
    여과The reaction mixture was filtered
  3. 3
    건조The filtrate was dried over K2CO3
  4. 4
    여과filtered
  5. 5
    농축concentrated
  6. 6
    기타The resultant oil was purified via flash chromatography (2-10% acetone in dichloromethane, 0.5% TEA gradient)

실험 절차

To a solution of triethylamineamine (2.0 mL, 14 mmol) in ethanol (20 mL) was added dimethylamine hydrochloride (1.63 g, 20 mmol), titanium tetraisopropoxide (5.96 mL, 20 mmol) and 3,4-dilinoleyloxybenzaldehyde (6.35 g, 10 mmol). The mixture was allowed to stir under argon for 10 h at room temperature. Sodium borohydride (0.57 g, 15 mmol) was added to the reaction mixture which was then allowed to stir at room temperature overnight. 6N Aqueous ammonia (30 mL), was added slowly to the reaction mixture followed by dichloromethane. The reaction mixture was filtered. The filtrate was dried over K2CO3, filtered and concentrated. The resultant oil was purified via flash chromatography (2-10% acetone in dichloromethane, 0.5% TEA gradient) to afford 4.94 g (74%) of a yellow oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07514099B2uspto-grants-2009_04