HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2,3,6-Trichlorobenzylideneaminooxyacetic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 2,3,6-Trichlorobenzaldehyde | HCID 20781 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Aminooxyacetic acid hemihydrochloride | HCID 2723609 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3,6-Trichlorobenzylideneaminooxyacetic Acid | HCID 131713327 | — |
Reaction Steps
A warm solution of 3.0 gm. (0.014 mole) of 2,3,6-trichlorobenzaldehyde in 50 ml. of ethanol was stirred into a warm solution of 1.6 gm. (0.015 equiv.) of carboxymethoxylamine hemihydrochloride and 0.7 gm. (0.008 mole) of anhyd. sodium acetate in 50 ml. water. Heating on the steam bath was maintained for one-half hour: then the reaction mixture was evaporated by 3/4 volume and was cooled. The solid present was removed by filtration, washed with water and dried in vacuum dessicator over phosphorus pentoxide to obtain 3.9 gm. (96.5%) of crude product melting at 159°-160° C. This material, twice recrystallized from aqueous-isopropyl alcohol, melted at 160°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04423241 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-5e8111f1141546d2afe8d8ea6c8beaef |
| Source note | uspto-grants-1983_12 |