Water → 2-Benzo[b]furan-3-ylethylamine
Reaction equation
[C:1]([CH2:3][C:4]1[C:5]2[CH:12]=[CH:11][CH:10]=[CH:9][C:6]=2[O:7][CH:8]=1)#[N:2].[H-].[Al+3].[Li+].[H-].[H-].[H-].O>C(OCC)C>[O:7]1[CH:8]=[C:4]([CH2:3][CH2:1][NH2:2])[C:5]2[CH:12]=[CH:11][CH:10]=[CH:9][C:6]1=2Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 3.97 grams (0.025 mole) of 3-cyanomethylbenzo[b]furan in 200 milliliters of diethyl ether was slowly added to a refluxing suspension of 3.84 grams (0.1 mole) of lithium aluminum hydride in 400 milliliters of ether and the mixture was heated 3 hours, then cooled and water was slowly added. The suspension was filtered and the filtrate was evaporated to obtain an oily product, the hydrochloride salt of which has m.p. 183°-185° C.
Workup
- temperaturethe mixture was heated 3 hours
- temperaturecooled
- filtrationThe suspension was filtered
- customthe filtrate was evaporated
- customto obtain an oily product
Sources & evidence
- ORD record
- ord-f636aa1af8874a8d9c033c4cbc0b1eb7
- Source dataset
- uspto-grants-1990_04
- Patent number
- US04916223
Reaction notes
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