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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Azatricyclo(3.3.1.1,3,7)decan-4-oneHCID 142642—
ReactantHCID 86623776HCID 86623776—
SolventEthanolHCID 702—
ProductHCID 87333855HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163915B2
Source datasetuspto-grants-2012_04
ORD IDord-ebd0e033bb824d7aa4a5b1643039efff
Source noteuspto-grants-2012_04