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HRID 349216作成日:2026年10月23日

Triethylamine → N-[(3-chlorophenyl)methyl]-1-azabicyclo[2.2.2]octan-3-amine

https://huagongshe.com/ja/reaction/349216

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-ChlorobenzaldehydeHCID 11477—
反応物Quinuclidine, 3-amino-, dihydrochlorideHCID 197853—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Sodium HydroxideHCID 14798—
生成物N-[(3-chlorophenyl)methyl]-1-azabicyclo[2.2.2]octan-3-amineHCID 1715896430%

反応手順

A mixture of of 3-aminoquinuclidine dihydrochloride (2.0 g, 10.0 mmol), NEt3 (1.3 mL) and 3-chlorobenzaldehyde (1.5 g, 11.0 mmol) in THF (50 mL) was stirred at room temperature. To this was added Na(OAc)3BH 13.2 g, 15 mmol) and the reaction was stirred overnight. The reaction mixture was diluted with 3N NaOH and water and extracted with EtOAc. The organic extracts were combined, washed with water and then brine and dried over K2CO3. The solution was filtered and the solvent was evaporated in vacuo to give an oil which was chromatographed on silica (94/6 CHCl3/0.5 M NH3 in MeOH). The appropriate fractions were combined and the solvent was evaporated in vacuo to give N-[(3-chlorophenyl)methyl]-1-azabicyclo[2.2.2]octan-3-amine (0.75 g, 30%) as an intermediate, a light yellow semi-solid. MH+=251,253. The 1H NMR was consistent with the assigned structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07179818B2
出典データセットuspto-grants-2007_02
ORD IDord-91f1822674c442d28b532453a12610e5
出典メモuspto-grants-2007_02