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Chemical Structure| 106889-84-3 Chemical Structure| 106889-84-3

Structure of 106889-84-3

Chemical Structure| 106889-84-3

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Product Details of [ 106889-84-3 ]

CAS No. :106889-84-3
Formula : C16H17NO
M.W : 239.31
SMILES Code : O=CCN(CC1=CC=CC=C1)CC2=CC=CC=C2
MDL No. :MFCD15516293

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Application In Synthesis of [ 106889-84-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 106889-84-3 ]

[ 106889-84-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 101-06-4 ]
  • [ 106889-84-3 ]
YieldReaction ConditionsOperation in experiment
General procedure: DMSO (3.92 mmol, 2 equiv.) was added dropwise to a stirred solution of oxalyl chloride (2.35 mmol, 1.2 equiv.) in CH2Cl2 (15 mL) under argon at -78 C and the reaction mixture was stirred for 5 min. Then a solution of 2-(dibenzylamino)alcohols 2a-d (1.96 mmol, 1 equiv.) in CH2Cl2 (1 mL) were added. After 30 min of stirring at -78 C triethylamine (7.8 mmol, 4 equiv.) was added, and mixtures were allowed to warm to room temperature over 30 min. The reaction mixtures were then diluted with H2O (30 mL) and CH2Cl2 (30 mL) and the layers were separated. The organic layers were washed with 1% HCl (10 mL), H2O (10 mL), 5% NaHCO3 (10 mL) and brine (10 mL), dried over MgSO4, filtrated and concentrated under reduced pressure. The resulting crude 2-(dibenzylamino)aldehydes 3a-d were used without additional purification.
To a solution of oxalyl chloride (6.95 g, 54.7 mmol) in dichloromethane (150 mL), a solution of dimethyl sulfoxide (9.26 g, 118.5 mmol) in dichloromethane (100 mL) was added dropwise at -70CC. After stirring for 30 mm at -70CC, a solution of 2-(dibenzylamino)ethanol (11 g, 45.58 mmol) in dichloromethane (150 mL) was added to thereaction mixture dropwise. After stirring for another 45 mi triethylamine (19.2 mL, 136.7mmol) was added dropwise and stirred at -70CC for 1.5h.Saturated sodium bicarbonate (200 mL) was added into the reaction mixture, which was extracted with dichloromethane (200 mL). Theorganic extracts were washed with brine (50 mL), dried over MgSO4 and concentrated invacuoto afford the 2-(dibenzylamino)acetaldehyde, which was immediately used in the nextstep.1H NMR (400 MHz, CDC13) oe 9.54 (t, J=1.5 Hz, 1H), 7.42 - 7.24 (m, 1OH), 3.71 (s, 4H),3.20 (d, J=1.5 Hz, 2H) ppm.
 

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