3-Hydroxybenzaldehyde → 3-Formylphenyl acetate
Reaction equation
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6].C(N(CC)CC)C.CN(C1C=CC=CN=1)C.[C:26](OC(=O)C)(=[O:28])[CH3:27]>ClCCl>[C:26]([O:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6])(=[O:28])[CH3:27]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
3-Hydroxybenzaldehyde (10 g., 81.88 mmol) was dissolved in 150 ml dichloromethane under argon. Triethylamine (17.12 ml, 0.123 mol) and dimethylaminopyridine (5 mg.) were added, and the resulting stirred solution was treated with acetic anhydride (8.5 ml, 90 mmol). After stirring for fifteen hours, the reaction mixture was transferred to a separatory funnel using an additional 50 ml dichloromethane. The organic layer was washed with water (2×100 ml) and concentrated to give a light brown oil weighing 14.85 g. Plug filtration through silica gel using dichloromethane furnished 13.3 g (quant.) of a light orange oil which was shown by NMR and IR to be pure enough for use in subsequent reactions (see Tables 3 and 7). ##STR34##
Workup
- stirringAfter stirring for fifteen hours
- customthe reaction mixture was transferred to a separatory funnel
- washThe organic layer was washed with water (2×100 ml)
- concentrationconcentrated
- customto give a light brown oil
- filtrationPlug filtration through silica gel
- customfurnished 13.3 g (quant.) of a light orange oil which
Sources & evidence
- ORD record
- ord-c0df5f77a26d40d2bdf87dc25135fd40
- Source dataset
- uspto-grants-1998_06
- Patent number
- US05763681
Reaction notes
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