돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 719110생성일: 2026년 10월 26일

Ninhydrin → Methyl (R)-2-Amino-3-(trimethylsilyl)propanoate

https://huagongshe.com/reaction/719110

반응식

참여 물질

역할이름HCID투입량
반응물NinhydrinHCID 10236—
반응물Sodium CarbonateHCID 10340—
반응물(2R)-2-amino-3-(trimethylsilyl)propanoic acidHCID 11008231—
반응물Boron, trifluoro(methanol)-, (T-4)-HCID 11062313—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매Dichloromethane methanolHCID 21226129—
생성물Methyl (R)-2-Amino-3-(trimethylsilyl)propanoateHCID 5930239792%

반응 조건

온도70 °C

반응 단계

3-Trimethylsilyl alanine (J. Organomet. Chem., 628, (2001), 183–194; 19 mg, 0.118 mmol) was mixed with 3 ml BF3-MeOH (14%, 3.7 mmol) in a sealed tube and heated to 70° C. Analysis was performed using TLC (MeOH:DCM 1:9, stained w. ninhydrine in ethanol). The mixture was heated for 3 h and was then cooled to ambient temperature. The mixture was poured into a mixture of 3 ml EtOAc and 2 ml water containing Na2CO3. More Na2CO3 (5%-aq) was added until pH ca 7. The aqueous phase was washed with EtOAc (2×3 ml). The combined organic layers were washed with brine (1 ml), dried with Na2SO4 and evaporated. The product was obtained as a white film. Mass: 19 mg (92% yield). NMR (CDCl3): 0.1 (s, 9H), 1.2–1.4 (m, 2H), 3.8 (s, 3H), 4.2 (brs, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07132416B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-5929ac61b44f44a68d65dad6554dcc85
출처 메모uspto-grants-2006_11