HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880111Generated: November 2, 2026
Water → 4-(2-Fluoropyridin-3-yl)cycloheptanone
https://huagongshe.com/reaction/1880111
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 4-(2-Fluoropyridin-3-yl)cyclohexanone | HCID 57606721 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(2-Fluoropyridin-3-yl)cycloheptanone | HCID 59327109 | — |
Reaction Steps
To a solution of boron trifluoride-diethyl etherate (0.64 g, 4.50 mmol) and 4-(2-fluoropyridin-3-yl)cyclohexanone (0.79 g, 4.09 mmol) in DCM (8 mL) at −25° C. under argon was added (trimethylsilyl)diazomethane (2.25 mL, 5.18 mmol, 2.0 M in hexanes). The reaction was stirred for 2 h at that temperature, water was added, and the mixture was extracted with DCM (2×). The combined organic extracts were washed with 10:1 saturated ammonium chloride/ammonium hydroxide mixture (1×), water (1×), saturated aqueous sodium chloride (1×), and dried over anhydrous magnesium sulfate. The mixture was filtered and the filtrate concentrated in vacuo. The resulting oil was purified by silica gel chromatography to give 4-(2-fluoropyridin-3-yl)cycloheptanone. MS (ESI, pos. ion) m/z: 208.1 (M+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-b081f6a8798a41458f897826243c0914 |
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| Source note | uspto-grants-2012_11 |
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