Basic information Safety Supplier Related

2-{4-[3-(dimethylamino)propoxy]phenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Basic information Safety Supplier Related

2-{4-[3-(dimethylamino)propoxy]phenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Basic information

Product Name:
2-{4-[3-(dimethylamino)propoxy]phenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Synonyms:
  • N,N-dimethyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]1-Propanamine
  • 2-{4-[3-(dimethylamino)propoxy]phenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 4-[3-(Dimethylamino)propoxy]benzene boronic acid, pinacol ester
  • N,N-Dimethyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]propan-1-amine
  • 1-Propanamine, N,N-dimethyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]-
  • 4-[3-(Dimethylamino)propoxy]phenylboronic acid, pinacol ester
CAS:
627899-90-5
MF:
C17H28BNO3
MW:
305.22
Mol File:
627899-90-5.mol
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2-{4-[3-(dimethylamino)propoxy]phenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Chemical Properties

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
color 
WHITE
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Safety Information

Hazard Codes 
C
Hazard Note 
Corrosive
HS Code 
2931900090
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2-{4-[3-(dimethylamino)propoxy]phenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane Usage And Synthesis

Synthesis

76579-64-1

61676-62-8

627899-90-5

GENERAL STEPS: To a 100 mL flame-dried two-neck flask was added 3-(4-bromophenoxy)-N,N-dimethyl-1-propanamine (3.0 g, 11.6 mmol) and freshly distilled tetrahydrofuran (80 mL). The resulting solution was cooled to -78 °C and n-butyllithium (8.7 mL, 13.9 mmol, 1.6 M hexane solution) was added dropwise over 10 min under nitrogen protection. The reaction mixture was stirred at -78 °C for 1 hour. Subsequently, isopropyl pinacol borate (2.6 g, 13.9 mmol) was quickly added and the resulting mixture was slowly warmed to room temperature for 24 hours. Upon completion of the reaction, the mixture was poured into 50 mL of water and extracted with chloroform (300 mL). The organic layers were combined, washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was removed by rotary evaporation and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/dichloromethane) to afford the target product as a light yellow oil (1.6 g, yield: 45.0%). The product was characterized as follows: 1H NMR (400 MHz, CDCl3, Me4Si): δ = 7.77 (d, 2H, J = 8.8 Hz), 6.90 (d, 2H, J = 8.8 Hz), 3.94 (t, 2H, J = 6.4 Hz), 2.46 (t, 2H, J = 6.8 Hz), 2.26 (s, 6H), 1.88 (m , 2H, J = 6.8 Hz), 1.25 (s, 12H).13C NMR (100 MHz, CDCl3, Me4Si): 161.57, 136.73, 113.41, 83.13, 74.40, 66.02, 54.09, 45.42, 27.43, 25.00.Calculated elemental analysis values ( C17H28BNO3): C, 66.90; H, 9.25; N, 4.59. Measured values: C, 66.73; H, 9.23; N, 4.63. IR (KBr, cm-1): 2981, 2936, 2816, 2716, 1566, 1463, 1281, 1245.

References

[1] Dyes and Pigments, 2015, vol. 113, p. 210 - 218
[2] Patent: KR2015/122308, 2015, A. Location in patent: Paragraph 0094; 0095; 0098; 0099

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