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HRID 1774721作成日:2026年10月25日

Hydrochloric Acid → 6-Bromo-1-methyl-1,2,3,4-tetrahydroquinolin-2-one

https://huagongshe.com/reaction/1774721

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Methyl iodideHCID 6328—
反応物6-Bromo-3,4-dihydroquinolin-2(1H)-oneHCID 14373281—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物6-Bromo-1-methyl-1,2,3,4-tetrahydroquinolin-2-oneHCID 6310614180%

反応条件

温度0 °C

反応手順

To a solution of 6-bromo-3,4-dihydroquinolin-2(1H)-one (5 g, 22.1 mmol) in DMF (100 mL) cooled to 0° C. was added potassium tert-butoxide (4.96 g, 44.2 mmol) portionwise and the reaction mixture was stirred at 0° C. for 15 min. Then, methyl iodide (4.08 g, 28.8 mmol) was added and the reaction mixture allowed to warm up to room temperature and stirring was continued over night. More MeI (1.25 g, 8.86 mmol) was added and the reaction mixture was heated to 40° C. until completion of the reaction. The mixture was diluted with EtOAc, poured into 100 mL of 1M HCl and the aqueous phase was extracted with EtOAc (2×200 mL). Combined organics were washed with brine, dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by silica gel flash chromatography eluting with a 0 to 30% EtOAc-heptane gradient to give the title compound (4.23 g, 80%) as an off white solid. MS: 240.0, 242.1 (M+H+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09260408B2
出典データセットuspto-grants-2016_02
ORD IDord-210de72cd4b042948351689e2034df96
出典メモuspto-grants-2016_02