HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299713Generated: October 25, 2026
Hydrochloric Acid → methyl E-2-hydroxyimino-2-(3-phenoxylphenyl)acetate
https://huagongshe.com/reaction/2299713
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Hydroxyimino-2-(3-phenoxyphenyl)acetonitrile | HCID 85308279 | — |
| Solvent | Water | HCID 962 | — |
| Product | methyl E-2-hydroxyimino-2-(3-phenoxylphenyl)acetate | HCID 86589771 | 33% |
Reaction Steps
A mixture of 2-hydroxyimino-2-(3-phenoxyphenyl)acetonitrile (3.00 g), potassium hydroxide (3.40 g), ethanol (15 ml) and water (15 ml) was heated under reflux for 24 hours. The reaction mixture was acidified with 1 N HCl, and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride, dried (MgSO4) and then concentrated. The reaction mixture was dissolved in methanol (30 ml), admixed with concentrated sulfuric acid (a catalytic amount), and then heated under reflux for 24 hours. The reaction mixture was combined with aqueous sodium bicarbonate and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride, dried (MgSO4) and then concentrated. The residue was subjected to column chromatography on silica gel to obtain methyl Z-2-hydroxyimino-2-(3-phenoxyphenyl)acetate (1.14 g, yield 33%) as an oil from a fraction eluted with ethyl acetate-hexane (1:2, v/v).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06495581B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-67c53a2e08644fa7b01b9d74d6be868a |
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| Source note | uspto-grants-2002_12 |
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