Sodium Chloride → HCID 19036612, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:21]=[CH:20][C:6]2[CH2:7][CH2:8][C:9]3[CH:10]=[CH:11][N:12]([CH2:14][CH2:15][NH:16][C:17](=[O:19])[CH3:18])[C:13]=3[C:5]=2[CH:4]=1.[OH-:22].[K+].[Cl-].[Na+].[CH2:26]([OH:29])[CH2:27]O.[OH2:30]>>[C:17]([OH:19])(=[O:30])/[CH:18]=[CH:27]/[C:26]([OH:29])=[O:22].[CH3:1][O:2][C:3]1[CH:21]=[CH:20][C:6]2[CH2:7][CH2:8][C:9]3[CH:10]=[CH:11][N:12]([CH2:14][CH2:15][NH2:16])[C:13]=3[C:5]=2[CH:4]=1Participants
Procedure
6.30 g of N-[2-(4,5-dihydro-8-methoxy-1H-benz[g]indol-1-yl)ethyl]-acetamide were heated to 140° for 21 hours under argon in 64 ml of ethylene glycol/water 2:1 in the presence of 7.40 g of potassium hydroxide. The reaction mixture was left to cool and was poured into 250 ml of semi-concentrated sodium chloride solution. The mixture was extracted three times with diethyl ether. The combined extracts were washed once with saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated. The crude product was dissolved in 100 ml of methanol and treated with 2.6 g of fumaric acid. The separated crystals were recrystallized from a total of 340 ml of methanol. 3.8 g (49%) of 2-(4,5-dihydro-8-methoxy-1H-benz[g]indol-1-yl)-ethylamine fumarate (1:1) were obtained as yellowish crystals with m.p. 183°-185°.
Workup
- waitThe reaction mixture was left
- temperatureto cool
- extractionThe mixture was extracted three times with diethyl ether
- washThe combined extracts were washed once with saturated sodium chloride solution
- dry with materialdried over sodium sulfate
- filtrationfiltered
- customevaporated
- dissolutionThe crude product was dissolved in 100 ml of methanol
- additiontreated with 2.6 g of fumaric acid
- customThe separated crystals were recrystallized from a total of 340 ml of methanol
Sources & evidence
- ORD record
- ord-c3914e9e16054cca8d35689674a908f1
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05646173
Reaction notes
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