HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585644Generated: October 30, 2026
Acetic Acid → (+/-)-n-{3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexyl}hydroxylamine
https://huagongshe.com/reaction/585644
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (+/-)-3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanone oxime | HCID 86586318 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (+/-)-n-{3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexyl}hydroxylamine | HCID 22337762 | — |
Reaction Steps
Borane (0.412 ml of a 1M solution in tetrahydrofuran) was added to a stirred solution of (±)-3-[2,4-bis(methoxymethoxy)phenyl]cyclohexanone oxime (85 mg) in tetrahydrofuran (2 ml) at 0° C. under argon. After 2 hr, acetic acid (1 ml) was added and the mixture was allowed to warm to ambient temperature. After 16 hr, sodium hydrogen carbonate (20 ml of a saturated aqueous solution) was added, the mixture was extracted with ethyl acetate (3×20 ml) and the combined organic extracts were dried over magnesium sulfate and evaporated in vacuo. The crude residue was purified by flash column chromatography (SiO2, dichloromethane/methanol, 9:1 v/v) to furnish two compounds as clear gums which were identified as diastereoisomers of the title compound; trans-isomer (12 mg, 14%) m/z (ES+) 312 (M+H)+; cis-isomer (0.017 g, 20%) m/z (ES+) 312 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933319B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-d19d6a26bf0945c7ada3d93a6b755d0a |
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| Source note | uspto-grants-2005_08 |
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