Formic Acid → HCID 14344237, compound
Reaction equation
[C:1]([OH:5])(=[O:4])[CH:2]=O.[CH2:6]([C:8]1[CH:14]=[CH:13][CH:12]=[C:11]([CH2:15][CH3:16])[C:9]=1[NH2:10])[CH3:7].[CH:17](O)=[O:18]>>[CH2:6]([C:8]1[CH:14]=[CH:13][CH:12]=[C:11]([CH2:15][CH3:16])[C:9]=1[N:10]([CH:17]=[O:18])[CH2:2][C:1]([OH:5])=[O:4])[CH3:7]Participants
4
Conditions
- Temperature
- 70 °C
Procedure
32.6 g (0.22 mole) of an approximately 50% strength aqueous glyoxylic acid solution were added dropwise to 14.9 g (0.10 mole) of 2,6-diethylaniline and 100 ml of formic acid at room temperature, with gentle warming. The mixture was stirred at 70° C. for 1 hour, with vigorous evolution of gas, the formic acid was distilled off up to an internal temperature of 120° C., the mixture was allowed to cool and was poured onto water and the solid was filtered off with suction and dired. 21.8 g of N-(2,6-diethylphenyl)-N-formylglycine of melting point 139-41° C. were obtained.
Workup
- distillationthe formic acid was distilled off up to an internal temperature of 120° C.
- temperatureto cool
- additionwas poured onto water
- filtrationthe solid was filtered off with suction
Sources & evidence
- ORD record
- ord-755d79a9d9f74f3b85acbbb7116e15c1
- Source dataset
- uspto-grants-1990_05
- Patent number
- US04925958
Reaction notes
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