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Chemical Structure| 763932-69-0 Chemical Structure| 763932-69-0

Structure of 763932-69-0

Chemical Structure| 763932-69-0

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Product Details of [ 763932-69-0 ]

CAS No. :763932-69-0
Formula : C13H19NO3
M.W : 237.30
SMILES Code : O=C(OC(C)(C)C)NC(C1=CC=C(O)C=C1)C
MDL No. :MFCD24467355

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* 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 [ 763932-69-0 ]

[ 763932-69-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 134855-87-1 ]
  • [ 763932-69-0 ]
YieldReaction ConditionsOperation in experiment
64% With triethylamine; In tetrahydrofuran; for 15.08h; 16) l-(4-[(2S)-2-methoxypropyl]oxy}phenyl)ethanamineA. fert-butyl [l-(4-hydroxyphenyl)ethyl]carbamateTo l-(4-hydroxyphenyl)ethanamine (0.96 g, 7.0 mmol) in THF (20 mL) triethylamine (2.9 mL, 21 mmol) was added followed by the addition of di-tert-butyl dicarbonate (1.8 g, 8.4 mmol) in THF (20 mL) during 5 minutes. The resulting mixture was stirred for 15 hours, the volatiles removed under reduced pressure and the residue purified by silica gel column chromatography using a gradient of heptanes : ethyl acetate 9:1 to 1:1 affording 1.1 g of the tert-butyl [l-(4-hydroxyphenyl)ethyl]carbamate (64 %). 1H NMR (400 MHz, DMSO- d6) delta ppm 9.18 (s, 1 H) 7.18 (d, J=7.78 Hz5 1 H) 7.03 - 7.11 (m, J=8.41 Hz5 2 H) 6.63 - 6.72 (m, 2 H) 4.45 - 4.56 (m, 1 H) 1.35 (s, 9 H) 1.25 (d, J=7.03 Hz5 3 H) MS (ESI) m/z: 238 [M+H]
With sodium hydroxide; In ethanol; water; at 20℃; for 4.5h; To a solution of <strong>[134855-87-1]4-(1-aminoethyl)phenol</strong> (1.0 g) in ethanol (24 mL) were added di-t-butyl dicarbonate (4.77 g) and sodium hydroxyde (146 mg) at 0C and the solution was stirred at room temperature for 4.5 hours. The reaction solution was concentrated and water was added thereto. The solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and concentrated. The obtained residue was purified by column chromatography on silica gel (hexane: ethyl acetate=7:1) to give the title compound (2.18 g) having the following physical data. TLC:Rf 0.88 (chloroform:methanol=5:1); NMR (CDCl3): delta 1.36-1.50 (m, 13H), 4.79 (m, 1H), 7.10-7.18 (m, 2H), 7.26-7.32 (m, 2H).
 

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