Ethanol hydrochloride → HCID 70189071, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][C:10]=1[O:11][CH3:12])/[C:7](=[CH:13]/[CH2:14][NH2:15])/[CH2:6][CH2:5]2.[ClH:16].C(O)C>>[ClH:16].[Br:1][C:2]1[CH:3]=[C:4]2[C:8]([C:7]([CH2:13][CH2:14][NH2:15])=[CH:6][CH2:5]2)=[CH:9][C:10]=1[O:11][CH3:12]Participants
3
Procedure
(E)-2-(5-Bromo-6-methoxyindan-1-ylidene)ethylamine (5.0 g, 18.6 mmol) was dissolved in saturated HCl/ethanol (200 ml) and the solution was refluxed for 2 hours. After cooling, the solvent was distilled off under reduced pressure and the resulting crystals were washed with diethyl ether to provide the title compound (yield 4.61 g, 81%).
Workup
- temperaturethe solution was refluxed for 2 hours
- temperatureAfter cooling
- distillationthe solvent was distilled off under reduced pressure
- washthe resulting crystals were washed with diethyl ether
Sources & evidence
- ORD record
- ord-fb9c0479f8634848ab81cac23ff26593
- Source dataset
- uspto-grants-1999_07
- Patent number
- US05922771
Reaction notes
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