Methanol → HCID 54267340, compound
Reaction equation
CO[CH2:3][C:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)=[O:5].[N:12]1[CH:17]=[CH:16][C:15]([CH:18]=O)=[CH:14][CH:13]=1.[OH-:20].[Na+].[CH3:22]O>>[CH3:22][O:20][C:11]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:4](=[O:5])[CH:3]=[CH:18][C:15]1[CH:14]=[CH:13][N:12]=[CH:17][CH:16]=1Participants
5
Procedure
The procedure is as in Example 11, starting from 15 g of 2-methoxyacetophenone and 20.4 g of pyridine-4-carbaldehyde in 50 ml of methanol and using 45 ml of a 2.5 N aqueous sodium hydroxide solution in place of the 11 N solution. 7 g of 1-(2-methoxyphenyl) 3-(4-pyridyl) 2-propene-1-one which melts at 70° C. are obtained.
Sources & evidence
- ORD record
- ord-7a23613ecdcd48d3b236ee4155a61aba
- Source dataset
- uspto-grants-1981_10
- Patent number
- US04294841
Reaction notes
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