戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 659182作成日:2026年10月26日

1,4-Dibromobutane → cis-(2-Pyrrolidin-1-yl-cyclohexyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/659182

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DibromobutaneHCID 8056—
反応物Potassium CarbonateHCID 11430—
反応物(1S,2R)-Cyclohexane-1,2-diamine, N1-BOC protectedHCID 1514389—
溶媒AcetonitrileHCID 6342—
生成物cis-(2-Pyrrolidin-1-yl-cyclohexyl)-carbamic acid tert-butyl esterHCID 6668088888.1%

反応手順

1-N-Boc-1,2-cis-cyclohexyldiamine 5 (CAS 184954-75-4) (1.65 g, 7.7 mmol) was dissolved in 100 mL acetonitrile. Potassium carbonate (5.3 g, 39 mmol) and 1,4-dibromobutane (2.8 g, 13 mmol) were added and the reaction mixture was refluxed overnight. The solvent was evaporated off. The residue was taken up in water and ethyl acetate and was extracted three times with ethyl acetate. The combined organic phases were dried on sodium sulfate, filtered and evaporated. Purification of the residue by flash chromatography on silica gel (dichloromethane/methanol/ammonia 100:0:0→140:10:1) yielded cis-(2-pyrrolidin-1-yl-cyclohexyl)-carbamic acid tert-butyl ester as a yellow liquid (1.82 g, 88%), MS: m/e=269.4 [(M+H)+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08080541B2
出典データセットuspto-grants-2011_12
ORD IDord-9cf38beef3ff40eebc6de1ccba63f616
出典メモuspto-grants-2011_12