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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 379097생성일: 2026년 10월 25일

Penicillamine → (2s)-2-Amino-3-methyl-3-((2,4,6-trimethoxyphenyl)methylthio)butanoic acid

https://huagongshe.com/reaction/379097

반응식

참여 물질

역할이름HCID투입량
반응물PenicillamineHCID 5852—
반응물Trifluoroacetic acidHCID 6422—
반응물2,4,6-Trimethoxybenzyl alcoholHCID 602515—
용매DichloromethaneHCID 6344—
생성물(2s)-2-Amino-3-methyl-3-((2,4,6-trimethoxyphenyl)methylthio)butanoic acidHCID 6977926095%

반응 조건

온도0 °C

반응 단계

A suspension of (2S)-2-amino-3-methyl-3-sulfanylbutanoic acid (5.0 g, 703 mmol) in CH2Cl2 (150 mL) was cooled to 0° C. Trifluoroacetic acid (54 mL, 703 mmol) was added dropwise over a period of 5 min. 2,4,6-trimethoxybenzyl alcohol (6.64 g, 34 mmol) in CH2Cl2 (137 mL) was added dropwise at 0° C. with stirring. The stirring was continued for 1 hour at 0° C. and 2 hours at room temperature, the solvent removed in vaciio and the residue was dried under high vacuum for 3 hours. The crude red solid was recrystallized from 1:1:1 CH2Cl2:MeOH:EtOAc to give the title compound 10.5 g (95 %) as a white solid which was used for the next step without further purification. 1H NMR (300 MHz, CDCl3) δ 6.10 (s, 2H), 3.84 (s, 6H), 3.76 (s, 3H), 3.40-4.10 (mult, 3H), 1.69 (s, 3H), 1.23 (s, 3H); mass spectrum (API-TIS) m/z 330 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06297260B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-14193dc265f24c76b847e1d36e918d25
출처 메모uspto-grants-2001_10