تفاعل #2075688

ord-69f4d2afe8434b96ae98abb8ad45137e

معادلة التفاعل

N
ammonia
CNC.Cl
dimethylamine hydrochloride
CCCCCCCC/C=C\CCCCCCCCOc1ccc(C=O)cc1OCCCCCCCC/C=C\CCCCCCCC
3,4-dioleyloxybenzaldehyde
[BH4-].[Na+]
Sodium borohydride
CCCCCCCC/C=C\CCCCCCCCOc1ccc(CN(C)C)cc1OCCCCCCCC/C=C\CCCCCCCC
N,N-Dimethyl-3,4-dioleyloxybenzylamine

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGto stir at room temperature overnight
  2. 2
    ترشيحThe reaction mixture was filtered
  3. 3
    غسيلthe solids washed with dichloromethane
  4. 4
    تجفيفThe filtrate was dried over K2CO3
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated
  7. 7
    أخرىThe resultant oil was purified via flash chromatography (2-10% acetone in dichloromethane, 0.5% TEA gradient)
  8. 8
    أخرىto afford 5.81 g (87-+%) of a yellow oil

الإجراء التجريبي

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-dioleyloxybenzaldehyde (6.39 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. Concentrated aqueous ammonia (4 mL) was added slowly to the reaction mixture. The reaction mixture was filtered and the solids washed with dichloromethane. 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 5.81 g (87-+%) of a yellow oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07641915B2uspto-grants-2010_01