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Chemical Structure| 245057-86-7 Chemical Structure| 245057-86-7

Structure of 245057-86-7

Chemical Structure| 245057-86-7

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Product Details of [ 245057-86-7 ]

CAS No. :245057-86-7
Formula : C14H17NO3
M.W : 247.29
SMILES Code : C=CC(N1CC2=C(C=C(OC)C(OC)=C2)CC1)=O
MDL No. :MFCD12091127
InChI Key :GEUWOWUYASBMCB-UHFFFAOYSA-N
Pubchem ID :43616276

Safety of [ 245057-86-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 245057-86-7 ]

* 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 [ 245057-86-7 ]

[ 245057-86-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 3382-18-1 ]
  • [ 814-68-6 ]
  • [ 245057-86-7 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In tetrahydrofuran; at 0 - 20℃; for 2h; To a stirring suspension of the 6,7-dimethoxy-3,4-dihydroisoquinolme (1 g, 5.2 mmol, 1 equiv.) and TEA (1800 .tL, 12.6 mmol, 2.5 equiv.) in anhydrous TFIF (10 mL) at 0 C was added acryloyl chloride (1320 jiL, 13.2 rnmol, 2.6 equiv.) and the reaction was allowed to slowly warm up to room temperature. After 2 hours, the mixture was diluted with CH2CI2 (2 x 50 mL) and washed with saturated brine (2 x 50 mL) and the combined organics were concentrated in vacua. The residue was taken up in 10% MeOH / C112C12 and purified by column chromatography to afford the title compound as a white solid (700 mg, 54%, mixture of E/Z isomers). ‘H NMR (500 MHz, Chlorofonn-d) 6 6.63 (in, 3H), 6.29 (d, J 16.8 Hz, IH), 5.69 (dd,J= 10.6,1.8Hz, IH), 4.69 (s, IH [major]), 4.63 (s, 0.8H [minor]), 3.82 (s, 711), 3.73 (t, J= 5.6 Hz, 1H), 2.84-2.77 (m, 2H); HRMS-ESI (m/z) calculated for C1J119N03 [M+H]:248.128; found: 248.1281.
With triethylamine; In tetrahydrofuran; at 0 - 20℃; for 2h; To a stirring suspension of the 6,7-dimethoxy-3,4-dihydroisoquinoline (1 g, 5.2 mmol, 1 equiv.) and TEA (1800 µL, 12.6 mmol, 2.5 equiv.) in anhydrous THF (10 mL) at 0 C was added acryloyl chloride (1320 µL, 13.2 mmol, 2.6 equiv.) and the reaction was allowed to slowly warm up to room temperature. After 2 hours, the mixture was diluted with CH2Cl2 (2 × 50 mL) and washed with saturated brine (2 × 50 mL) and the combined organics were concentrated in vacuo. The residue was taken up in 10% MeOH / CH2Cl2 and purified by column chromatography to afford the title compound as a white solid (700 mg, 54%, mixture of E/Z isomers). 1H NMR (500 MHz, Chloroform-d) δ 6.63 (m, 3H), 6.29 (d, J = 16.8 Hz, 1H), 5.69 (dd, J = 10.6, 1.8 Hz, 1H), 4.69 (s, 1H [major]), 4.63 (s, 0.8H [minor]), 3.82 (s, 7H), 3.73 (t, J = 5.6 Hz, 1H), 2.84 - 2.77 (m, 2H); HRMS-ESI (m/z) calculated for C14H18NO3 [M+H]: 248.128; found: 248.1281. 2
 

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