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HRID 217264作成日:2026年10月25日

Azobisisobutyronitrile → Methyl 3-(bromomethyl)thiophene-2-carboxylate

https://huagongshe.com/reaction/217264

反応式

関与物質

役割名称HCID仕込み量
反応物AzobisisobutyronitrileHCID 6547—
反応物N-bromobutanimideHCID 67184—
反応物Methyl 3-methylthiophene-2-carboxylateHCID 580757—
溶媒Carbon TetrachlorideHCID 5943—
生成物Methyl 3-(bromomethyl)thiophene-2-carboxylateHCID 1053769368.6%

反応手順

A mixture of methyl 3-methylthiophene-2-carboxylate (13.2 mmol), N-Bromosuccinimide (13.2 mmol) and a catalytic amount of azobis-isobutyronitrile in carbon tetrachloride were heated at reflux under nitrogen. The reaction mixture was irradiated with a 500 W UV lamp for 1.5 hours, cooled down to room temperature and then filtered under autocup 0.45 μm, followed by the evaporation of the filtrate. The residue was purified by chromatography on silica gel (eluent: stepwise gradient of 3-5% diethyl ether in petroleum ether) to give 2.13 g of Intermediate IV.1 (69%), which was characterized by 1H NMR (CDCl3, 400 MHz) δ (ppm) 3.90 (s, 3H), 4.92 (s, 2H), 7.18 (d, J=5.3 Hz, 1H), 7.47 (d, J=5.3 Hz, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193372B2
出典データセットuspto-grants-2012_06
ORD IDord-570703af8cd14b91be69f2555fbda542
出典メモuspto-grants-2012_06