HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450677Generated: October 31, 2026
Cyclohexanone Oxime → 3-[(Cyclohexylideneamino)oxy]propanoic acid
https://huagongshe.com/reaction/1450677
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclohexanone Oxime | HCID 7517 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[(Cyclohexylideneamino)oxy]propanoic acid | HCID 19977209 | 24,503% |
Reaction Steps
A mixture of 32.8 g (0.29 mol) of cyclohexanone oxime, 26 g (0.26 mmol) of ethyl acrylate, 26 ml (0.052 mol) of a 2N solution of KOH in ethanol and 150 ml of ethanol is stirred for 96 hours at 60° C. and afterwards concentrated on a vacuum rotary evaporator. The residue (an orange oil) is dissolved in 175 g (0.31 tool) of a 10% solution of KOH in ethanol and the solution is heated for 1 hour to 60° C. The solvent is distilled off and the solid residue is taken up in water. After acidification with c. 15 ml of conc. hydrochloric acid and extraction with ethyl acetate, the organic phase is washed with water, dried over Na2SO4 and concentrated on a vacuum rotary evaporator. Distillation of the residue yields 11.8 g (25%) of the desired acid as an orange liquid. The boiling point is 135° C./0.05 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05602196 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-2f76d6ee00514261b05b6fa40148cab8 |
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| Source note | uspto-grants-1997_02 |
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