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HRID 719806作成日:2026年10月27日

Thionyl Chloride → 3-(1-Acetyl-4-piperidinyl)propionyl chloride

https://huagongshe.com/reaction/719806

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物3-(1-Acetylpiperidin-4-yl)propanoic acidHCID 9855751—
生成物3-(1-Acetyl-4-piperidinyl)propionyl chlorideHCID 10465951—

反応手順

3-(1-Acetyl-4-piperidinyl)propionic acid (10.0 g) was added by portions to thionyl chloride (30 ml) at room temperature. After stirring at room temperature for 30 minutes, thionyl chloride was evaporated under reduced pressure to give the crude product of 3-(1-acetyl-4-piperidinyl)propionyl chloride. Aluminum chloride (20 g) was added by portions to a suspension of the crude product and 2,2,2-trifluoro-N-(2-methoxyphenyl)acetamide (10.0 g) at room temperature. After stirring at room temperature for 1 hour, the reaction mixture was poured into ice (200 g), extracted with ethyl acetate, and washed with brine. The organic layer was dried over anhydrous magnesium sulfate, the solvent was evaporated under reduced pressure, the resulting residue was purified by silica gel chromatography (eluting solvent; ethyl acetate), and the solvent was evaporated to give the title compound as colorless crystals (8.83 g) having a melting point of 77 to 79° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07132547B2
出典データセットuspto-grants-2006_11
ORD IDord-738cd10ed35a438994a764590553a0b3
出典メモuspto-grants-2006_11