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HRID 44173作成日:2026年10月25日

Methyl iodide → 6-Bromo-1-methyl-1,2,3,4-tetrahydroquinolin-2-one

https://huagongshe.com/reaction/44173

反応式

関与物質

役割名称HCID仕込み量
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Hydrochloric AcidHCID 313—
溶媒DimethylformamideHCID 6228—
生成物6-Bromo-1-methyl-1,2,3,4-tetrahydroquinolin-2-oneHCID 6310614178%

反応手順

To a solution of 6-bromo-3,4-dihydro-1H-quinolin-2-one (339 mg, 1.50 mmol) in 15 ml dry DMF was added potassium tert-butylate (336 mg, 3.0 mmol). After the mixture was stirred for 30 min at room temperature, a solution of methyl iodide (426 mg, 3.0 mmol) in 5 ml dry DMF was added. Following overnight stirring, the mixture was diluted with 100 ml 1 N HCl. Extraction with ethyl acetate (2×100 mL) followed by washing of the organic extracts with water and brine, drying over MgSO4 and removal of the solvent in vacuo gave a light yellow solid. Purification by flash chromatography (hexanes/ethyl acetate, 7/3, Rf=0.21) gave 6-bromo-1-methyl-3,4-dihydro-1H-quinolin-2-one (281 mg, 1.17 mmol, 78%) as colorless needles.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541404B2
出典データセットuspto-grants-2013_09
ORD IDord-e20cbb289c6144fe82b0f57c0a437507
出典メモuspto-grants-2013_09