戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 4278作成日:2026年10月25日

Methyl Thioglycolate → Methyl 3-amino-5-chloro-2-thiophenecarboxylate

https://huagongshe.com/reaction/4278

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl ThioglycolateHCID 16907—
反応物SodiumHCID 5360545—
反応物3,3-DichloroacrylonitrileHCID 11535554—
溶媒MethanolHCID 887—
生成物Methyl 3-amino-5-chloro-2-thiophenecarboxylateHCID 14050402—

反応手順

In a flame dried flask under a nitrogen atmosphere, and with mechanical stirring, a solution of about 1.2 g (0.05 mole) of sodium metal dissolved in 30 ml of dry methanol was treated dropwise with 2.35 g (1.98 ml, 0.022 mole) of methyl thioglycolate while maintaining the temperature below 25° C. A solution of 2.70 g (0.022 mole) of 3,3-dichloroacrylonitrile [R. L. Soulen, D. B. Clifford, F. F. Crim and J. A. Johnston, J. Org. Chem. 36 (22), 3386-3391 (1971)] and 10 ml of methanol was then added dropwise at a rate such as to keep the reaction temperature <28° C. The reaction mixture became cloudy and orange. Stirring was continued for an hour. The mixture was concentrated under reduced pressure, was diluted with water, and was extracted five times with 60 ml portions of chloroform. The combined extracts were dried over anhydrous magnesium sulfate, filtered, and evaporated under reduced pressure to furnish an oil which was chromatographed under moderate pressure ("flash" chromatography) on a column of silica gel (Woelm 32-63 micrometers, i.d. 5 cm×height 18 cm); the eluant was isopropyl ether; 15 ml fractions were taken. Fractions 15-20 were combined and evaporated to give methyl 3-amino-5-chloro-2-thiophenecarboxylate as a colorless solid: m.p. 99°-101° C.; yield 0.60 g (14%); ir (KBr) 3448 cm-1, 3343, 1674, 1615, 1546, 1455, 1425 along others; 1H-nmr (CDCl3) delta 3.8 ppm (s, 3H), 5.3 (broad s, 2H), 6.4 (s, 1H); mass spectrum 191 (molecular ion), 159 (-32, CH3OH, parent peak) and others.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04725599
出典データセットuspto-grants-1988_02
ORD IDord-6e4b65d842a24b1fb016b47316612e80
出典メモuspto-grants-1988_02