Hydrochloric Acid → HCID 19600204, compound
Reaction equation
[O:1]1[CH2:5][CH2:4][N:3]=[C:2]1[C:6]1[O:27][C:9]2[CH2:10][N:11]([C:14](=[O:26])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:12][CH2:13][C:8]=2[CH:7]=1.[ClH:28]>C(OCC)C.CO>[ClH:28].[O:1]1[CH2:5][CH2:4][N:3]=[C:2]1[C:6]1[O:27][C:9]2[CH2:10][N:11]([C:14](=[O:26])[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH2:12][CH2:13][C:8]=2[CH:7]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 0.148 g of 1-[2-(2-oxazolin-2-yl)-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl]-6-phenylhexan-1-one in 10 ml of diethyl ether, 0.5 ml of about 10% hydrogen chloride in methanol was added, followed by stirring for 10 minutes, after which the solvent was distilled off under reduced pressure. The resulting crude product was crystallized from diethyl ether to yield the desired product.