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HRID 8428作成日:2026年10月23日

Hydrochloric Acid → Methyl (2S)-2-(2,3,4-trifluoroanilino)propionate

https://huagongshe.com/ja/reaction/8428

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物2,6-LutidineHCID 7937—
反応物Trifluoromethanesulfonic acidHCID 62406—
反応物2,3,4-TrifluoroanilineHCID 77468—
反応物(+)-Methyl lactateHCID 637514—
溶媒DichloromethaneHCID 6344—
生成物Methyl (2S)-2-(2,3,4-trifluoroanilino)propionateHCID 1012521090%

反応手順

Under ice-cooling, methyl D-lactate (8.5 g) and 2,6-lutidine (11.4 g) were dissolved in dichloromethane (100 ml). After dropping anhydrous trifluoromethanesulfonic acid (25.4 g), the mixture was heated to room temperature and stirred for 30 minutes. Then it was cooled to 0° C. again and a solution (30 ml) of 2,3,4-trifluoroaniline (12.0 g) in dichloromethane was dropped therein to. The mixture was stirred at the same temperature for 17 hours. To the resultant solution, hydrochloric acid (0.5 mol/l) was added and the mixture was extracted with dichloromethane. The extract was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and filtered. After evaporating the solvent, the residue thus obtained was subjected to silica gel column chromatography. Thus, 17.1 g (90%) of the title compound was obtained as an oily substance. The optical purity determined by HPLC was 97% ee.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087778B2
出典データセットuspto-grants-2006_08
ORD IDord-22db996d591f4d78a18857d82c7798ef
出典メモuspto-grants-2006_08