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HRID 1873530作成日:2026年10月26日

Benzyl Chloride → 5-Benzyl-5-cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide

https://huagongshe.com/reaction/1873530

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl ChlorideHCID 7503—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 68626191—
溶媒TetrahydrofuranHCID 8028—
生成物5-Benzyl-5-cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamideHCID 6862583646%

反応手順

5-Cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 12a (4.0 g, 19.3 mmol) was dissolved in 60 mL of tetrahydrofuran with stirring followed by addition of benzyl chloride (5.4 g, 42.5 mmol) and lithium hexamethyldisilazide (42.5 mL, 42.5 mmol) under nitrogen atmosphere. The reaction mixture was stirred at room temperature for 4 hours. The reaction was monitored by TLC until the disappearance of the starting materials and quenched with 50 mL of water. The mixture was extracted with ethyl acetate. The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound 5-benzyl-5-cyano-hexahydro-cyclopenta[c]pyrrole-2-carboxylic acid dimethylamide 14a (2.6 g, yield 46%) as a light yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08304411B2
出典データセットuspto-grants-2012_11
ORD IDord-3e3f96bb650d4e3ea07703794bdff18a
出典メモuspto-grants-2012_11