Acetic Anhydride → HCID 13340163, compound
Reaction equation
[C:1]([O:4][C:5]1[C:6]([CH3:26])=[N+:7]([O-])[C:8]([CH:11]([O:21][C:22](=[O:24])[CH3:23])[CH2:12][N:13]([C:17]([CH3:20])([CH3:19])[CH3:18])[C:14](=[O:16])[CH3:15])=[CH:9][CH:10]=1)(=[O:3])[CH3:2].[C:27]([O:30]C(=O)C)(=[O:29])[CH3:28].C(=O)(O)[O-].[Na+]>C(OCC)(=O)C>[C:1]([O:4][C:5]1[C:6]([CH2:26][O:30][C:27](=[O:29])[CH3:28])=[N:7][C:8]([CH:11]([O:21][C:22](=[O:24])[CH3:23])[CH2:12][N:13]([C:17]([CH3:20])([CH3:19])[CH3:18])[C:14](=[O:16])[CH3:15])=[CH:9][CH:10]=1)(=[O:3])[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1.0 g. (0.0027 mole) of 3-acetoxy-2-methyl-6-[1-acetoxy-2-(N-tert-butylacetamido)ethyl]pyridine N-oxide in 10 ml. of acetic anhydride was heated at the reflux temperature for 2.5 hours, then was allowed to cool to room temperature and stirred at this temperature overnight. The reaction mixture was poured into a two phase mixture of ethyl acetate and aqueous sodium bicarbonate and stirred for 1 hour. The organic layer was separated, dried over anhydrous magnesium sulfate, filtered and evaporated to dryness in vacuo to give a brown oil which was purified by column chromatography on silica gel with ether as the eluant to give 300 mg. (27%) of the desired product; m.p. 60°-64° C.
Workup
- stirringstirred for 1 hour
- customThe organic layer was separated
- dry with materialdried over anhydrous magnesium sulfate
- filtrationfiltered
- customevaporated to dryness in vacuo
- customto give a brown oil which
- customwas purified by column chromatography on silica gel with ether as the eluant
- customto give 300 mg
Sources & evidence
- ORD record
- ord-dd303eba22914ac3928097f6eb997ad5
- Source dataset
- uspto-grants-1984_10
- Patent number
- US04477671
Reaction notes
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