戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1701332作成日:2026年10月27日

Acetic Acid → 4-(((5-Chloro-2thienyl)methyl)amino)-benzoic acid

https://huagongshe.com/reaction/1701332

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物4-Aminobenzoic AcidHCID 978—
反応物N-boranyl-N-methylmethanamineHCID 74604—
反応物2-Thiophenecarboxaldehyde, 5-chloro-HCID 81700—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物4-(((5-Chloro-2thienyl)methyl)amino)-benzoic acidHCID 20347826—

反応条件

温度40 °C

反応手順

A mixture containing 46.6 grams (0.34 moles) of p-aminobenzoic acid, 50 grams (0.34 moles) of 5-chloro-2-thiophenecarboxaldehyde and 400 ml. of toluene was heated to reflux for about three and a half hours. The water formed was collected in a Dean-Stark trap. The reaction mass was cooled at the end of this period and the Schiff base collected as a tan solid. To a mixture of the intermediate Schiff base and 1.2 liters of glacial acetic acid 21.2 grams (0.36 moles) of dimethylaminoborane was added. The reaction mass was warmed to 40° C. for about 30 minutes and poured in 2 liters of ice water. The white precipitate of 4-(((5-chloro-2-thienyl)methyl)amino)benzoic acid was washed in water, dried, and recrystallized from toluene. The melting point was 177°-178° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04192884
出典データセットuspto-grants-1980_03
ORD IDord-ad488bf1274642eaaa6e1e919907b224
出典メモuspto-grants-1980_03