Acetic Anhydride → HCID 86604276, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][C:6]([C:12]([CH3:16])([CH3:15])[CH2:13][OH:14])=[CH:5][C:4]=1[N+:17]([O-:19])=[O:18].[C:20](OC(=O)C)(=[O:22])[CH3:21]>C(Cl)Cl.CN(C1C=CN=CC=1)C>[CH3:1][O:2][C:3]1[C:4]([N+:17]([O-:19])=[O:18])=[CH:5][C:6]([C:12]([CH3:16])([CH3:15])[CH2:13][O:14][C:20](=[O:22])[CH3:21])=[CH:7][C:8]=1[N+:9]([O-:11])=[O:10]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
2-(4-Methoxy-3,5-dinitro-phenyl)-2-methyl-propan-1-ol was dissolved in 5 mL of CH2Cl2. Acetic anhydride was added followed by DMAP. The mixture was stirred overnight, then diluted in 15 mL of CH2Cl2 and washed with 1 M NaSO4, saturated NaHCO3, and brine. The CH2Cl2 solution was then dried with Na2SO4, filtered, and concentrated to provide acetic acid 2-(4-methoxy-3,5-dinitro-phenyl)-2-methyl-propyl ester (628 mg) as a brown oil.
Workup
- washwashed with 1 M NaSO4, saturated NaHCO3, and brine
- dry with materialThe CH2Cl2 solution was then dried with Na2SO4
- filtrationfiltered
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-a8cb817b3ae549c3830d73a7e302f0c2
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07214802B2
Reaction notes
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