HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880116Generated: November 1, 2026
Sodium Hydroxide → 4-(2-Fluoropyridin-3-yl)cyclohexanone oxime
https://huagongshe.com/reaction/1880116
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | hydroxylamine-O-sulfonic acid | HCID 76284 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-(2-Fluoropyridin-3-yl)cyclohexanone | HCID 57606721 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(2-Fluoropyridin-3-yl)cyclohexanone oxime | HCID 59326817 | — |
Reaction Steps
A suspension of aminooxysulfonic acid (0.35 g, 3.11 mmol) in 96% formic acid (2.5 mL) was added dropwise to a solution of 4-(2-fluoropyridin-3-yl)cyclohexanone (0.50 g, 2.59 mmol) in 96% formic acid (2.5 mL) at room temperature. The solution was stirred for 15 min, then warmed to 40° C. for 2 h, then cooled 0° C. Ethyl acetate (10 mL) was added and the mixture was neutralized by the dropwise addition of 10 N aqueous sodium hydroxide solution (10 mL) followed by saturated aqueous sodium bicarbonate. The resulting biphasic mixture was separated, the aqueous layer was extracted with ethyl acetate (2×), and the combined extracts were dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The resulting oil was purified by silica gel chromatography to give 4-(2-fluoropyridin-3-yl)cyclohexanone oxime. [M+1]=209.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318718B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-1480d890789542de9f999b4384ed1485 |
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| Source note | uspto-grants-2012_11 |
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