ChemicalBook--->CAS DataBase List--->1187160-18-4

1187160-18-4

1187160-18-4 Structure

1187160-18-4 Structure
IdentificationBack Directory
[Name]

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

1187160-18-4
[Synonyms]

7-METHOXY-2,3-DIHYDRO-1H-INDEN-1-AMINE HCL
7-METHOXY-2,3-DIHYDRO-1H-INDEN-1-AMINE HYDROCHLORIDE
2,3-DIHYDRO-7-METHOXY-1H-INDEN-1-AMINE HYDROCHLORIDE
[Molecular Formula]

C10H14ClNO
[MDL Number]

MFCD25562962
[MOL File]

1187160-18-4.mol
[Molecular Weight]

199.677
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

7-METHOXY-2,3-DIHYDRO-1H-INDEN-1-AMINE HYDROCHLORIDE(1187160-18-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

1H-Inden-1-one, 2,3-dihydro-7-methoxy-, oxime

908108-58-7

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

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
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