HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Chloro-6-fluorobenzylideneaminooxyacetic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2-Chloro-6-fluorobenzaldehyde | HCID 67847 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Aminooxyacetic acid hemihydrochloride | HCID 2723609 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-6-fluorobenzylideneaminooxyacetic Acid | HCID 131713329 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04423241 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-355e24221fb747d4a80019e3eea9bb25 |
| Source note | uspto-grants-1983_12 |