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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2219792생성일: 2026년 10월 24일

Water → (R)-3-(4-Methoxybenzyl)-2-oxothiazolidine-4-carboxylic Acid

https://huagongshe.com/ko/reaction/2219792

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium CarbonateHCID 11430—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물3-Mercapto-2-(4-methoxy-benzylamino)-propionic acidHCID 11021047—
용매AcetonitrileHCID 6342—
생성물(R)-3-(4-Methoxybenzyl)-2-oxothiazolidine-4-carboxylic AcidHCID 11207876—

반응 조건

온도40 °C

반응 단계

A 22 L three-necked round bottom flask fitted with an internal temperature probe and a mechanical stirrer was charged with 3-mercapto-2-(4-methoxybenzylamino)-propionic acid (400.0 g, 1.66 mol), potassium carbonate (480.0 g, 3.47 mol) and 2.80 L of water. The mixture was heated at 40° C. with stirring until it became homogeneous and was then cooled to 20-25° C. A solution of N,N-carbonyldiimidazole (400.0 g, 222.47 mol) in 2.8 L of acetonitrile was added while maintaining an internal reaction temperature of less than 30° C. The reaction was monitored by HPLC and was complete upon the disappearance of starting material. The acetonitrile was removed by distillation at 40° C. and 80-100 torr. Iso-propyl acetate (200 mL) was added and the pH of the mixture was adjusted to 2 with 150 mL of 3M H2SO4. The biphasic mixture was filtered, separated and the organic layer azeotropically dried by distillation at atmospheric pressure. The final measured water content was less than 0.5%. The resulting solution was further diluted with 1.8 L of iso-propyl acetate and used in the next example. 1H NMR (300 MHz, DMSO) δ 7.15 (d, 8.3 Hz, 2H), 6.88 (d, 8.3 Hz, 2H), 4.52 (AB, JAB=15.5 Hz, ΔvAB=238.4 Hz, 2H), 4.31-4.24 (m, 1H), 3.71 (s, 3H), 3.67-3.59 (m, 1H), 3.36-3.28 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07414137B2
출처 데이터셋uspto-grants-2008_08
ORD IDord-18e4a78682614b3894f1082fad314314
출처 메모uspto-grants-2008_08