戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 477868作成日:2026年10月26日

Triethylamine → dimethyl N-(2-fluoro-4-iodobenzoyl)-L-glutamate

https://huagongshe.com/reaction/477868

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Thionyl ChlorideHCID 24386—
反応物2-Fluoro-4-iodobenzoic acidHCID 2774516—
反応物Dimethyl L-glutamate hydrochlorideHCID 12917568—
触媒DimethylformamideHCID 6228—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒BenzeneHCID 241—
溶媒DichloromethaneHCID 6344—
生成物dimethyl N-(2-fluoro-4-iodobenzoyl)-L-glutamateHCID 1472061174%

反応手順

To 20 mL of benzene are added 2.0 g (0.00752 mol) of 2-fluoro4-iodobenzoic acid, followed by 2.3 mL (320 mmol) of thionyl chloride and several drops of dimethylformamide. The mixture is heated at reflux of 3.5 hours. The solvent is then removed in vacuo and the residue pumped dry. The resulting acid chloride is redissolved in 10 ml of methylene chloride, and added dropwise to cooled mixture of 1.67 g (7.89 mmol) of L-glutamic acid dimethyl ester hydrochloride, 5 mg of 4-dimethylaminopyridine, and 2.2 mL (15.8 mmol) of triethylamine in 30 mL of methylene chloride. After the addition, the reaction stirred at room temperature for 18 hours. The reaction mixture is then diluted with additional methylene chloride, washed with 1N hydrochloric acid, water and 5% sodium bicarbonate and dried over sodium sulfate. The solvent is removed in vacuo to give 2.34 g (74%) of dimethyl N-(2-fluoro-4-iodobenzoyl)-L-glutamate as a white solid m.p. 94°-96° C.; IR (KBr, cm-1)=1159, 1177, 1194, 1208, 1229, 1398, 1437, 1477, 1537, 1601, 1642, 1728, 1739, 1756, 3326.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04889859
出典データセットuspto-grants-1989_12
ORD IDord-42430265d92c41e7a5c2bd056593e131
出典メモuspto-grants-1989_12