戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2212527作成日:2026年10月27日

Potassium Carbonate → 5-(4-Bromo-but-2-enyloxy)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2212527

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物N-Boc-5-HydroxyindolineHCID 10657398—
反応物1,4-Dibromobut-1-eneHCID 53629311—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物5-(4-Bromo-but-2-enyloxy)-2,3-dihydro-indole-1-carboxylic acid tert-butyl esterHCID 6951507831.9%

反応条件

温度50 °C

反応手順

514 mg (2.3 mmol) 5-Hydroxy-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester in 12 ml DMF were treated with 830 mg (6 mmol) powdered K2CO3 and 1070 mg (5 mmol) 1,4-dibromobutene. The suspension was stirred at 50° C. for 3 h, cooled to RT, diluted with ether and water. The aqueous phase was extracted with ether, the organic phases were washed with water and dried over Na2SO4. Column chromatography on silica gel with hexane/EtOAc 9:1 yielded 270 mg (31%) 5-(4-Bromo-but-2-enyloxy)-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester as colorless solid, MS: 368 (MH+, 1Br).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07102007B2
出典データセットuspto-grants-2006_09
ORD IDord-fa12095754984bc18bb2b8a6b6e67c0b
出典メモuspto-grants-2006_09