HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697440Generated: October 31, 2026
1-Azatricyclo(3.3.1.1,3,7)decan-4-one → HCID 87333855, compound
https://huagongshe.com/reaction/1697440
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Azatricyclo(3.3.1.1,3,7)decan-4-one | HCID 142642 | — |
| Reactant | HCID 86623776 | HCID 86623776 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 87333855 | HCID 87333855 | — |
Reaction Steps
Solid O-(perfluorobenzyl)hydroxylamine HCl (167 mg, 0.669 mmol, Aldrich Chemical Co.) was added to a warm solution of 1-azatricyclo[3.3.1.13,7]decan-4-one (102 mg, 0.675 mmol) (prepared as reported in: Becker, D. P. and Flynn, D. L. Synthesis 1992, 1080-1082) in ethanol (1 mL). The mixture was swirled with warming to dissolve all solids. The nearly colorless solution was allowed to cool to room temperature overnight. The solvent was removed under vacuum, and the residue was crystallized from 10% ethanol in ethyl acetate (3 mL) to provide the title compound as hydrochloride salt. 1H NMR (300 MHz, CD3OD) δ 1.87-2.06 (m, 2 H), 2.22 (q, J=3 Hz, 1 H), 2.24-2.37 (m, 2 H), 2.83 (s, 1H), 3.30, (m, 1H), 3.43-3.57 (m, 2 H), 3.64 (s, 2 H), 3.66-3.78 (m, 2 H), 5.15-5.24 ppm (m, 2 H); MS (DCI/NH3) m/z 347 (M+H)+; Anal. C16H15N2OF5—HCl requires C, 50.21; H, 4.21; N, 7.32. Found C, 50.20; H, 3.99; N, 7.22.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163915B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-ebd0e033bb824d7aa4a5b1643039efff |
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| Source note | uspto-grants-2012_04 |
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