反应 #2075689

ord-b179739b4c5f49bf907ded43f7306c73

反应方程式

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
收率 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
收率 74.4%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGto stir at room temperature overnight
  2. 2
    过滤The reaction mixture was filtered
  3. 3
    干燥The filtrate was dried over K2CO3
  4. 4
    过滤filtered
  5. 5
    浓缩concentrated
  6. 6
    其他The resultant oil was purified via flash chromatography (2-10% acetone in dichloromethane, 0.5% TEA gradient)

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07641915B2uspto-grants-2010_01