HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905371Generated: October 30, 2026
Sodium Hydroxide → HCID 131713330, compound
https://huagongshe.com/reaction/905371
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Aminooxyacetic acid hemihydrochloride | HCID 2723609 | — |
| Reactant | 3-Chloro-2-methylbenzaldehyde | HCID 13162662 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131713330 | HCID 131713330 | — |
Reaction Steps
A warm solution of 1.5 gm. (0.01 mole) of 6-chloro-o-tolualdehyde in 15 ml. of ethanol was stirred into a solution of 1.1 gm. (0.010 equiv.) of carboxymethoxylamine hemihydrochloride and 1.3 gm. (0.016 equivs.) of anhyd. sodium acetate in 15 ml. water. After heating a half hour on the steam bath, the reaction mixture was cooled and adjusted to pH 8 with 5% aqueous sodium hydroxide. The mixture was extracted with ether, and the ether extract was discarded. The alkaline-aqueous phase was then adjusted to pH 5 with hydrochloric acid and was evaporated to 25 ml. volume. It was then acidified to pH 1.5-2.0 with cooling in ice bath. The solid was removed by filtration, was washed with cold water, and was dried in air to obtain 1.5 gm. (68%) of crude product melting at 121°-6° C. Recrystallization from aqueous-ethanol yielded 1.4 gm. of product melting at 124°-7° C. (dried at 65° C. in vacuo).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04423241 |
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| Source dataset | uspto-grants-1983_12 |
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| ORD ID | ord-e2165db2e5a04fea8e6ae898656d965b |
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| Source note | uspto-grants-1983_12 |
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