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HRID 131261作成日:2026年10月27日

Azobisisobutyronitrile → 6-Bromomethyl-nicotinic acid methyl ester

https://huagongshe.com/reaction/131261

反応式

関与物質

役割名称HCID仕込み量
反応物AzobisisobutyronitrileHCID 6547—
反応物HexaneHCID 8058—
反応物N-bromobutanimideHCID 67184—
反応物Methyl 6-methylnicotinateHCID 231548—
溶媒Carbon TetrachlorideHCID 5943—
生成物6-Bromomethyl-nicotinic acid methyl esterHCID 1275223735.5%

反応手順

To a solution of methyl 6-methylnicotinate (6.3 g) in carbon tetrachloride (100 mL) is added successively N-bromosuccinimide (8.9 g) and 2,2′-azobisisobutyronitrile (342 mg), and the mixture is refluxed under heating for 6 hours. After cooling to room temperature, to the reaction mixture is added n-hexane (300 mL) and the insoluble materials are removed by filtration. The filtrate is concentrated in vacuo and the resultant crude product is purified by column chromatography on silica gel (Solvent; n-hexane:ethyl acetate=10:1) and stirred in n-hexane to give methyl 6-(bromomethyl)nicotinate (3.4 g, yield; 35%) as colorless crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384952B2
出典データセットuspto-grants-2008_06
ORD IDord-88834c4755c14761a72f39e7f625bef1
出典メモuspto-grants-2008_06