Dimethylformamide → Methyl 2-(2-formylphenoxy)acetate
Reaction equation
[CH:1](=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[OH:4].C(=O)([O-])[O-].[K+].[K+].CN(C)C=O.Cl[CH2:22][C:23]([O:25][CH3:26])=[O:24]>O>[CH:1]([C:2]1[CH:8]=[CH:7][CH:6]=[CH:5][C:3]=1[O:4][CH2:22][C:23]([O:25][CH3:26])=[O:24])=[O:9]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 65 °C
Procedure
2. Approximately 509 g of the starting compound, salicylaldehyde (1) was introduced into a 4-liter Eriemeyer flask with powdered potassium carbonate (569 g), dimethylformamide (1,000 ml), and methyl chloroacetate (478 g) and mechanically stirred at 65° C. for about 24 hours. The stirring was stopped and the reaction mixture cooled to 25° C. The mixture was poured into cold water (0° C.) while stirring vigorously. An oil separated that suddenly solidified. Stirring was continued for 30 minutes and the solid isolated by filtration. The product was washed with water (2×1,000 ml) and pressed dry. The product can also be dried in vacuo at 25° C. A small sample (approx. 2 g) was purified by distillation. The boiling range of the pure product is 124°-128° C. at 2 mm Hg and has a melting temperature range of about 50.2°-50.6° C.
Workup
- temperaturethe reaction mixture cooled to 25° C
- stirringwhile stirring vigorously
- customAn oil separated
- stirringStirring
- waitwas continued for 30 minutes
- customthe solid isolated by filtration
- washThe product was washed with water (2×1,000 ml)
- custompressed dry
- customThe product can also be dried in vacuo at 25° C
- distillationA small sample (approx. 2 g) was purified by distillation
- customis 124°-128° C. at 2 mm Hg
- customa melting temperature range of about 50.2°-50.6° C.
Sources & evidence
- ORD record
- ord-25c1ed2d66ff46288e75956b10bcbaed
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05440054
Reaction notes
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