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 | HCID 2728340 | HCID 2728340 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131728690 | HCID 131728690 | 55% |
Reaction Steps
2-Bromo-3-hydroxy-cylohex-2-enone (80.0 g, 420 mmol) is added to a mechanically stirred reactor followed by methanol (300 mL). To the mixture is then added trimethyl orthoformate (186 mL, 1.70 mol, 4 eq) and sulfuric acid (9 mL). The resulting mixture is stirred for 2 h until completion and hydroxylamine sulfate (34.4 g, 210 mmol, 0.5 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 (˜1100 g). The precipitate formed is collected by filtration (filter 10 cm diameter, 1.5 cm cake thickness, <1 min total filtration time) rinsed with heptane (200 mL) and dried under nitrogen flow for 4-6 h to provide 50.8 g, (55% yield) of 2-bromo-3-methoxy-cylohex-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-4df5652527384c58b96d5b3f4b874312 |
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| Source note | uspto-grants-2011_02 |
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