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CAS No. : | 3382-18-1 | MDL No. : | MFCD00266748 |
Formula : | C11H13NO2 | Boiling Point : | - |
Linear Structure Formula : | C9H7(OCH3)2N | InChI Key : | NSLJVQUDZCZJLK-UHFFFAOYSA-N |
M.W : | 191.23 | Pubchem ID : | 30058 |
Synonyms : |
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Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P280-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302+H312+H332-H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* 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.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
36% | for 5 h; Reflux | (2-Acetyl-4-methyl-pentyl)-trimethyl-ammonium iodide (800 mg, 2.55 mmol, 1.00 equiv) was added to a solution of 6,7-dimethoxy- 3,4-dihydroisoquinoline (100 mg, 2.62 mmol, 1.00 equiv) and ethanol (10 mL). The resulting solution was heated at reflux for about 5 hours, and then water (20 mL) was added. Following standard extractive workup with dichloromethane (3 x 50 mL), the crude residue was purified by silica gel column chromatography (ethyl acetate / petroleum ether (1:4)) to afford the title compound as a white solid (300 mg, yield = 36percent). 1Η NMR (300 MHz, CDCl3), δ 6.63 (s, IH), 6.55 (s, IH), 3.89 (s, 3H), 3.83 (s, 3H), 3.55 (s, IH), 3.22-3.28 (m, IH), 2.94-3.14 (m, 4H), 2.31-2.65 (m, 4H), 1.73-1.81 (t, IH , J = 11.4), 1.33-1.39 (m, IH), 0.996-1.067 (t, IH, J = 10.5), 0.79-0.85 (m, 6H) LC-MS : m/z = 318(MH)+. |