Hydrochloric Acid → HCID 15117892, compound
Reaction equation
O1CCCCC1[O:7][CH2:8][CH2:9][O:10][CH2:11][CH2:12][O:13][C:14]1[CH:21]=[CH:20][C:19]([C:22]([CH2:25][C:26]([CH3:29])([CH3:28])[CH3:27])([CH3:24])[CH3:23])=[CH:18][C:15]=1[CH:16]=[O:17].Cl>CO>[OH:7][CH2:8][CH2:9][O:10][CH2:11][CH2:12][O:13][C:14]1[CH:21]=[CH:20][C:19]([C:22]([CH2:25][C:26]([CH3:29])([CH3:28])[CH3:27])([CH3:23])[CH3:24])=[CH:18][C:15]=1[CH:16]=[O:17]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The above benzaldehyde was dissolved in methanol (400 ml) containing 1N hydrochloric acid (50 ml) and the mixture was stirred at room temperature for 3 hours. The methanol was removed by evaporation in vacuo, and the residue was extracted with dichloromethane. The extracts were evaporated in vacuo, to give the title compound as an oil (23.6 g).
Workup
- customThe methanol was removed by evaporation in vacuo
- extractionthe residue was extracted with dichloromethane
- customThe extracts were evaporated in vacuo
Sources & evidence
- ORD record
- ord-99be7ac57efe4fd2a0924b0ebc72a347
- Source dataset
- uspto-grants-1990_06
- Patent number
- US04935442
Reaction notes
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