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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 458158생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/458158

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2,6-LutidineHCID 7937—
반응물Trifluoromethanesulfonic acidHCID 62406—
반응물2,3,4-TrifluoroanilineHCID 77468—
반응물(+)-Methyl lactateHCID 637514—
용매DichloromethaneHCID 6344—
생성물Methyl (2S)-2-(2,3,4-trifluoroanilino)propionateHCID 1012521090%

반응 단계

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 thereinto. 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07189847B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-5234169ef35346aaae211ebdd1ddbd8a
출처 메모uspto-grants-2007_03