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HRID 900757作成日:2026年10月26日

Methanesulfonyl chloride → 4-Benzoyl-1-methanesulphonylpiperidine

https://huagongshe.com/reaction/900757

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonyl chlorideHCID 31297—
反応物DiisopropylethylamineHCID 81531—
反応物4-Benzoylpiperidine hydrochlorideHCID 2724437—
溶媒DichloromethaneHCID 6344—
生成物4-Benzoyl-1-methanesulphonylpiperidineHCID 16043536—

反応手順

Neat DIPEA (1.54 ml, 8.86 mmol) was added dropwise to a solution of phenyl(4-piperidinyl)methanone hydrochloride (1 g, 4.43 mmol) in CH2Cl2 (20 ml) at 0° C. Then, neat MsCl (377 μL, 4.87 mmol) was slowly added and the cooling bath was removed. After 30 minutes, the reaction was quenched with water and diluted with CH2Cl2. After separation, the organic phase was washed with brine, dried over MgSO4 and evaporated to dryness. The final ketone 1 was obtained as a white solid (1.16 g, 98%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07361668B2
出典データセットuspto-grants-2008_04
ORD IDord-aa78a692c2cb4f939b8c603d3c78b629
出典メモuspto-grants-2008_04