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HRID 49443作成日:2026年10月26日

Dimethyl Sulfoxide → 1-(4-Methylbenzyl)piperidin-4-one

https://huagongshe.com/reaction/49443

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfoxideHCID 679—
反応物TriethylamineHCID 8471—
反応物Ammonium ChlorideHCID 25517—
反応物Oxalyl chlorideHCID 65578—
反応物1-(4-Methylbenzyl)piperidin-4-olHCID 791482—
溶媒DichloromethaneHCID 6344—
生成物1-(4-Methylbenzyl)piperidin-4-oneHCID 1195954181%

反応手順

To 2.8 mL (32 mmol) of oxalyl chloride in 75 mL of CH2Cl2 at −78° C. was added 4.6 mL (64 mmol) of DMSO. To this mixture was added 5.3 g (26 mmol) of 1-(4-methylbenzyl)-4-piperidinol 123 in 10 mL of CH2Cl2, and the mixture was stirred 5 min in the cold. The mixture was quenched with 18 mL (129 mmol) of triethylamine and allowed to come to room temperature, and saturated aqueous ammonium chloride was added. The organic phase was washed with water and brine, dried, and evaporated to give 4.27 g (81%) of 1-(4-methylbenzyl)-4-piperidinone (124), which was used as is without further purification. GC/MS showed 100% purity with a molecular ion of 203.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706740B2
出典データセットuspto-grants-2004_03
ORD IDord-fb7270a74cbc4031b8e83c2f70138da2
出典メモuspto-grants-2004_03