돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1698769생성일: 2026년 10월 24일

Potassium Carbonate → (R)-2-((tert-Butoxycarbonyl)amino)-3-((2-nitrophenyl)amino)propanoic acid

https://huagongshe.com/ko/reaction/1698769

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-Fluoro-2-nitrobenzeneHCID 73895—
반응물3-Amino-N-(tert-butoxycarbonyl)-D-alanineHCID 7020984—
용매DimethylformamideHCID 6228—
생성물(R)-2-((tert-Butoxycarbonyl)amino)-3-((2-nitrophenyl)amino)propanoic acidHCID 5451259899%

반응 조건

온도70 °C

반응 단계

To a solution of 2-fluoronitrobenzene (3.45 g) in N,N-dimethylformamide (60 mL), (R)-(−)-2-tert-butoxycarbonylamino-3-amino-propionic acid (5 g) and potassium carbonate (6.77 g) were added, followed by stirring overnight at 70° C. The reaction mixture was allowed to cool down, poured into ice water, and then extracted with ethyl acetate. After 1 N hydrochloric acid was added to the aqueous layer to adjust pH to 3, the aqueous layer was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was then evaporated under reduced pressure. n-Hexane was added to the residue to for crystallization. The resultant crystals were collected by filtration, whereby the title compound (7.9 g) was obtained. Yield: 99%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06344452B1
출처 데이터셋uspto-grants-2002_02
ORD IDord-19f5d793898a4c83b763ac3eed7429f5
출처 메모uspto-grants-2002_02