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HRID 2212591作成日:2026年10月25日

Water → 7-bromo-1-propyl-4,4,6-trimethyl-3,4-dihydro-1H-quinoline-2-one

https://huagongshe.com/reaction/2212591

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium HydroxideHCID 14797—
反応物1-IodopropaneHCID 33643—
反応物7-Bromo-4,4,6-trimethyl-3,4-dihydro-1H-quinoline-2-oneHCID 21966423—
溶媒Dimethyl SulfoxideHCID 679—
生成物7-bromo-1-propyl-4,4,6-trimethyl-3,4-dihydro-1H-quinoline-2-oneHCID 21966426115.2%

反応条件

温度0 °C

反応手順

A mixture of powdered potassium hydroxide (1.26 g, 22.38 mmol) in DMSO (40 mL) was stirred at 0° C. for 10 min. 7-bromo-4,4,6-trimethyl-3,4- dihydro-1H-quinoline-2-one (Example 1e) (3.0 g, 11.19 mmol) was added cautiously, followed immediately by the addition of 1-iodopropane (5.5 mL, 55.95 mmol). The reaction mixture was warmed up to room temperature and stirred overnight at room temperature. The reaction mixture was poured into water and extracted with dichloromethane washed with water and brine, dried (MgSO4), filtered and evaporated to give 4.0 g of 7-bromo-1-propyl-4,4,6-trimethyl-3,4-dihydro-1H-quinoline-2-one and used without further purification in the Suzuki coupling (step a). 1H NMR (300 MHz; CDCl3): 0.98 (t, J=7.5 Hz,1 H), 1.26 (s, 6 H), 1.65 (t, J=7.5 Hz, 1 H), 2.37 (s, 3 H), 2.46 (s, 2 H), 3.88 (t, J=7.8 Hz, 2 H), 7.13 (s, 1 H), 7.15 (s, 1 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07102000B2
出典データセットuspto-grants-2006_09
ORD IDord-19f8755c4259480d81d941cfea1486da
出典メモuspto-grants-2006_09