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HRID 491550作成日:2026年10月27日

1,1-Dimethoxyethyl(dimethyl)amine → 4-(2-Oxopropyl)pyridine-3-carbonitrile

https://huagongshe.com/reaction/491550

反応式

関与物質

役割名称HCID仕込み量
反応物1,1-Dimethoxyethyl(dimethyl)amineHCID 87835—
反応物4-Methyl-3-cyanopyridineHCID 227806—
溶媒DimethylformamideHCID 6228—
生成物4-(2-Oxopropyl)pyridine-3-carbonitrileHCID 2191977569%

反応手順

A solution of 4-methyl-3-cyanopyridine (4 g, 33.9 mmol) and N,N-dimethylacetamide dimethylacetal (5.4 g, 40.6 mmol) in dry DMF (20 ml) was stirred at 130° for 7 h. The volatiles were removed in vacuo to afford a dark oil which solidified on standing. This material was chromatographed (SiO2; 50% EtOAc/Hexane—100% EtOAc) affording the title compound as an off-yellow solid (3.73 g, 69%). δH (CDCl3) 8.87 (1H, s), 8.74 (1H, d, J 5.2 Hz), 7.28 (1H, d, J 5,2 Hz), 4.00 (2H, s) and 2.36 (3H, s); m/z (ES+, 70V) 161 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07531549B2
出典データセットuspto-grants-2009_05
ORD IDord-723e890102d143da9e52bbf6d28febd7
出典メモuspto-grants-2009_05