HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018129Generated: October 30, 2026
Hydrochloric Acid → HCID 178521499, compound
https://huagongshe.com/reaction/1018129
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178476495 | HCID 178476495 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178521499 | HCID 178521499 | 31.5% |
Reaction Steps
At 20° C., 5.28 g (0.02 mol) of 2-(3-hydroxyimino-3H-benzofuran-2-ylideneaminooxy)-ethyl acetate (XVI-1) in 20 ml of dimethylformamide are stirred with 4.24 g (0.048 mol) of 45% strength aqueous sodium hydroxide solution for 3 hours. The mixture is acidified with 2 N hydrochloric acid and extracted with ethyl acetate, the organic phase is dried over sodium sulphate and the solvent is distilled off under reduced pressure. According to HPLC analysis, the crude product contains 23.4% of the stereoisomer A and 4.1% of the stereoisomer B of benzofuran-2,3-dione2-[O-(2-hydroxy-ethyl)-oxime]3-oxime (X-1). Stirring the crude product with diethyl ether affords 1.4 g (28.5% of theory) of crystalline benzofuran-2,3-dione2-[O-(2-hydroxy-ethyl)-oxime]3-oxime (X-1) consisting of 84.7% of stereoisomer A and 6% of stereoisomer B (HPLC).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06479675B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-8b8ecc732aec449bac3246612d8b5f71 |
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| Source note | uspto-grants-2002_11 |
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