Basic information Safety Supplier Related

7-METHOXY-2,3-DIHYDRO-1H-INDEN-1-AMINE HYDROCHLORIDE

Basic information Safety Supplier Related

7-METHOXY-2,3-DIHYDRO-1H-INDEN-1-AMINE HYDROCHLORIDE Basic information

Product Name:
7-METHOXY-2,3-DIHYDRO-1H-INDEN-1-AMINE HYDROCHLORIDE
Synonyms:
  • 2,3-DIHYDRO-7-METHOXY-1H-INDEN-1-AMINE HYDROCHLORIDE
  • 7-METHOXY-2,3-DIHYDRO-1H-INDEN-1-AMINE HCL
  • 7-METHOXY-2,3-DIHYDRO-1H-INDEN-1-AMINE HYDROCHLORIDE
CAS:
1187160-18-4
MF:
C10H14ClNO
MW:
199.67726
Mol File:
1187160-18-4.mol
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7-METHOXY-2,3-DIHYDRO-1H-INDEN-1-AMINE HYDROCHLORIDE Chemical Properties

storage temp. 
Sealed in dry,Room Temperature
Appearance
White to off-white Solid
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7-METHOXY-2,3-DIHYDRO-1H-INDEN-1-AMINE HYDROCHLORIDE Usage And Synthesis

Synthesis

908108-58-7

1187160-18-4

7-Methoxyindan-1-one oxime (2.92 g, 16 mmol) was dissolved in acetic acid (150 mL) and the hydrogenation reaction was carried out using an H-cube hydrogenation reactor under the following conditions set at a flow rate of 1 mL/min, a temperature of 80 °C, a pressure of 100 bar, and a catalyst of 10% Pd/C. Upon completion of the reaction, the solvent in the reaction mixture was removed by evaporation and the residue was dissolved in methanol, followed by the addition of 1 equiv. of hydrochloric acid in methanol. The solvent was evaporated again and the resulting residue was ground with ether to give 7-methoxy-1-aminoindan hydrochloride (2.38 g, 12 mmol, 75% yield). Electrospray mass spectrometry (ESMS) showed m/z 147 ([M + H]+).

References

[1] Patent: WO2010/71846, 2010, A2. Location in patent: Page/Page column 160

7-METHOXY-2,3-DIHYDRO-1H-INDEN-1-AMINE HYDROCHLORIDESupplier

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