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HRID 62217作成日:2026年10月25日

Benzene → Benzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylate

https://huagongshe.com/reaction/62217

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物Methyl vinyl ketoneHCID 6570—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
反応物Benzyl 4-formylpiperidine-1-carboxylateHCID 2776272—
生成物Benzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylateHCID 2343573257.2%

反応手順

Benzyl 4-formylpiperidine-1-carboxylate (5.17 g, 20.907 mmol) and p-Toluenesulfonic acid monohydrate (0.398 g, 2.091 mmol) were stirred in Benzene (30.0 ml, 334.136 mmol) at 70° C. But-3-en-2-one (3.76 ml, 41.813 mmol) was added and the reaction mixture was refluxed o/n while removing water with dean-stark trap. After cooling the reaction mixture to rt, sat. NaHCO3 soln. was added and the organic layer was dried over Na2SO4 and evaporated. The resulting oil was purified by Biotage (SiO2, 250 g, EtOAc/Hep 10% to 50%) to afford the title compound (3.58 g, 11.96 mmol, 57.2% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09446046B2
出典データセットuspto-grants-2016_09
ORD IDord-7f02d74748974695a9ee031a838a2b47
出典メモuspto-grants-2016_09