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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8454생성일: 2026년 10월 25일

Hydrochloric Acid → 2-(2,3,4-Trifluoroanilino)propionic acid

https://huagongshe.com/reaction/8454

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물Methyl (2R)-2-(2,3,4-trifluoroanilino)propionateHCID 10149157—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylacetamideHCID 31374—
생성물2-(2,3,4-Trifluoroanilino)propionic acidHCID 2201586698.3%

반응 단계

Potassium tertiary-butoxide (123.4 mg) was suspended in DMAc (2 ml). Under ice-cooling, a solution of methyl (2R)-2-(2,3,4-trifluoroanilino)propionate (223 mg, 91% ee) in DMAc (2 ml) was added thereto. The liquid reaction mixture was stirred at the same temperature for 1 hour. Then an aqueous solution of sodium hydroxide (3 mol/l; 2 ml) was added and the mixture was stirred for 1 hour. The liquid reaction mixture was adjusted to pH 2 with an aqueous solution of hydrochloric acid (3 mol/l) and then extracted with IPE. The organic layer was dried over anhydrous magnesium sulfate and evaporated. The crude product thus obtained was recrystallized from a solvent mixture of methylene chloride with normal hexane to thereby give the title compound (206 mg) as colorless crystals. The optical purity of this product was 0% ee. Various spectral data of this product was identical with those obtained in Example 23.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087778B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-61b34c6c1be54403acdd2d511f0f11ed
출처 메모uspto-grants-2006_08