Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Hydroxylamine, sulfate (1:1) | HCID 159255 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Cyclohexen-1-one, 3-hydroxy-2-methyl- | HCID 7057962 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86625062 | HCID 86625062 | 92% |
Reaction Steps
3-Hydroxy-2-methyl-cyclohex-2-enone (500 g, 3.96 mol) is added to a mechanically stirred reactor. To this is added methanol (1.35 L) followed by trimethyl orthoformate (1.65 L, 15.85 mol, 4 eq) and sulfuric acid (15 mL). The resulting mixture is stirred for 2 h until completion and hydroxylamine sulfate (275 g, 3.96 mol, 1 eq) is added as a solid. The mixture is heated to 40° C. and stirred at that temperature until complete conversion (2-2.5 h). The solution is then cooled to 5° C. and the pH is adjusted to 7 with saturated sodium bicarbonate (˜3 L). The precipitate formed is collected by filtration (filter 10 cm diameter, 1.5 cm cake thickness, <3 min total filtration time), rinsed with heptane (400 mL) and dried under nitrogen flow for 4-6 h to provide 560 g (92% yield) of 3-methoxy-2-methyl-cyclohex-2-enone oxime.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884246B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-9456b066809e437e823fb1b122d0dc55 |
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| Source note | uspto-grants-2011_02 |
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