HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803765Generated: October 31, 2026
O-Methylhydroxylamine hydrochloride → HCID 136359357, compound
https://huagongshe.com/reaction/1803765
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | HCID 14501412 | HCID 14501412 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 136359357 | HCID 136359357 | — |
Reaction Steps
Methoxylamine hydrochloride (4.14 g, 49.5 mmol) was added to a solution of Example 16C (9.69 g, 45.0 mmol) in pyridine (40 mL), and mixture was stirred overnight at ambient temperature. Only one regioisomer, 7-(trifluoromethyl)-2,3-dihydroquinolin-4(1H)-one was converted to the oxime. The mixture was concentrated under reduced pressure and ethyl acetate (300 mL) was added. The organic layer was washed twice with water (300 mL) and brine, dried over sodium sulfate, and concentrate under reduced pressure. The residue was chromatographed on silica gel eluting with 20-70% ethyl acetate in hexane to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 2.70 (t, J=6.61 Hz, 2H), 3.19 (td, J=6.53, 1.86 Hz, 2H), 3.90 (s, 3H), 6.57 (s, 1H), 6.82 (dd, J=8.14, 1.70 Hz, 1H), 6.97 (s, 1H), 7.79 (d, J=8.14 Hz, 1H). MS (DCI) m/z 245.05 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08350083B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-a96d131f87494ebda95f519625a66592 |
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| Source note | uspto-grants-2013_01 |
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