戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 32563作成日:2026年10月25日

Formamide → {(3-Iodophenyl)[(4-methylphenyl)sulfonyl]methyl}formamide

https://huagongshe.com/reaction/32563

反応式

関与物質

役割名称HCID仕込み量
反応物FormamideHCID 713—
反応物ChlorotrimethylsilaneHCID 6397—
反応物3-IodobenzaldehydeHCID 252610—
反応物2-Methylbenzene-1-sulfinic acidHCID 12661295—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒AcetonitrileHCID 6342—
溶媒tert-Butyl methyl etherHCID 15413—
生成物{(3-Iodophenyl)[(4-methylphenyl)sulfonyl]methyl}formamideHCID 8592970351%

反応条件

温度50 °C

反応手順

Trimethylsilylchloride (9.1 mL) was added to a stirred solution of 3-iodobenzaldehyde (15.1 g) and formamide (6.5 mL) in MeCN (34 mL) and toluene (34 mL) under an inert atmosphere. The reaction was then heated at 50° C. for 5 hours. Toluene sulfinic acid (15.3 g) was added and the reaction mixture was heated at 50° C. for a fisher 5 hours. The reaction mixture was cooled to ambient temperature, methyl t-butylether (55 mL) was added and stirred for 5 minutes. Water (275 mL) was added, the reaction cooled to 0° C. and stirred for 1 hour. The solid was filtered and the reaction flask was washed with MTBE (2×35 mL) and poured over the filtered cake. The solid was dried in a vacuum oven at 60° C. for 10 hours to afford impure title compound as a solid (14 g, 51%) which was used without further purification. A small sample was crystallised from EtOH;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427616B2
出典データセットuspto-grants-2008_09
ORD IDord-6f7c7740c4974382bd848d9d695a005a
出典メモuspto-grants-2008_09