Diazomethane → HCID 19902813, compound
Reaction equation
[N+](=[CH2:3])=[N-].[C:4]([C:7]1[NH:17][C:16](=[O:18])[CH:15]=[CH:14][C:8]=1[C:9]([O:11][CH2:12][CH3:13])=[O:10])(=[O:6])[CH3:5]>CCOCC>[C:4]([C:7]1[N:17]=[C:16]([O:18][CH3:3])[CH:15]=[CH:14][C:8]=1[C:9]([O:11][CH2:12][CH3:13])=[O:10])(=[O:6])[CH3:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
An ethereal solution of diazomethane (excess) is added to a stirred suspension of ethyl 1,6-dihydro-2-acetyl-6-oxonicotinate (2.20 g, 10.5 mmol) in 10 ml of ether. The ether and excess diazomethane are removed under vacuum, and the crude product is purified by column chromatography, eluting with 30% ethyl acetate/hexane to give ethyl 2-acetyl-6-methoxynicotinate.
Workup
- customThe ether and excess diazomethane are removed under vacuum
- customthe crude product is purified by column chromatography
- washeluting with 30% ethyl acetate/hexane
Sources & evidence
- ORD record
- ord-0d1ea0ec2dab409e8595b6a9383b89fe
- Source dataset
- uspto-grants-1992_03
- Patent number
- US05098466
Reaction notes
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