戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 591346作成日:2026年10月27日

Hydrochloric Acid → Hydrochloric Acid

https://huagongshe.com/reaction/591346

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Trifluoroacetic acidHCID 6422—
反応物HexaneHCID 8058—
反応物Tert-butyl 4-(6-fluoroindolin-1-yl)piperidine-1-carboxylateHCID 89613009—
溶媒DichloromethaneHCID 6344—
生成物Hydrochloric AcidHCID 313—
生成物6-Fluoro-1-(piperidin-4-yl)indolineHCID 22038384—

反応手順

To a solution of tert-butyl 4-(6-fluoroindolin-1-yl)piperidine-1-carboxylate (16.64 g, 52 mmol) in CH2Cl2 (45 mL) was added TFA (30 mL) slowly at room temperature. The resulting mixture was stirred at room temperature for 3 h. The resulting mixture was concentrated to remove most of solvent and TFA. The resulting residue was partitioned in CH2Cl2/H2O (100 mL/50 mL) and stirred. 3N NaOH(aq) was added slowly until the pH value of aqueous layer was >11. The aqueous layer was then extracted with CH2Cl2 (100 mL×10). The combined CH2Cl2 layer was dried (Na2SO4) and filtered. The solvent was removed by roto-evaporator, the resulting residue was dissolved in Et2O (100 mL) and 1N HCl (1M in Et2O, 60 mL, 60 mmol) was added slowly at 0° C. Then, the resulting mixture was allowed to warm to room temperature for another 30 min. Hexane (100 mL) was added and stirred for 15 min. The resulting white solid was filtered and washed with 50% Et2O/hexane (30 mL×3), then dried to yield 6-fluoro-1-(piperidin-4-yl)indoline as a white HCl salt.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09238658B2
出典データセットuspto-grants-2016_01
ORD IDord-190dc9512be14a81b03f30338c7d34ce
出典メモuspto-grants-2016_01