Ethanol → 2-Chloro-6-fluorobenzylideneaminooxyacetic Acid
Reaction equation
Cl[C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([F:10])[C:3]=1[CH:4]=O.C(O)C.[ClH:14].[C:15]([CH2:18][O:19][NH2:20])([OH:17])=[O:16].C(CON)(O)=O.C([O-])(=O)C.[Na+]>O>[Cl:14][CH:18]([O:19][N:20]=[CH:4][C:3]1[C:6]([F:10])=[CH:7][CH:8]=[CH:9][CH:2]=1)[C:15]([OH:17])=[O:16]Participants
6
Procedure
A warm solution of 2.0 gm. (0.013 mole) of 2-chloro-6-fluorobenzaldehyde in 40 ml. of ethanol was stirred into a warm solution of 1.4 gm. (0.013 equiv.) of carboxymethoxylamine hemihydrochloride and 0.6 gm. (0.007 mole) of anhyd. sodium acetate in 40 ml. of water. The mixture was heated a half-hour on the steam bath, and was then evaporated to dryness under reduced pressure to yield an oil, which was induced to crystallize by vigorous stirring. The solid material was triturated under water, removed by filtration, washed with water and dried in air to obtain 2.7 gm. (92.5%) of crude product melting from 95°-115° C. Recrystallization from n-heptaine/isopropyl alcohol gave 2.0 gm. of product melting at 116°-118° C.
Workup
- temperatureThe mixture was heated a half-hour on the steam bath
- customwas then evaporated to dryness under reduced pressure
- customto yield an oil, which
- customto crystallize by vigorous stirring
- customThe solid material was triturated under water
- customremoved by filtration
- washwashed with water
- customdried in air
- customto obtain 2.7 gm
- custommelting from 95°-115° C
- customRecrystallization from n-heptaine/isopropyl alcohol
- customgave 2.0 gm
Sources & evidence
- ORD record
- ord-355e24221fb747d4a80019e3eea9bb25
- Source dataset
- uspto-grants-1983_12
- Patent number
- US04423241
Reaction notes
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