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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Penicillamine | HCID 5852 | — |
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | 2,4,6-Trimethoxybenzyl alcohol | HCID 602515 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (2s)-2-Amino-3-methyl-3-((2,4,6-trimethoxyphenyl)methylthio)butanoic acid | HCID 69779260 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06297260B1 |
|---|
| 출처 데이터셋 | uspto-grants-2001_10 |
|---|
| ORD ID | ord-14193dc265f24c76b847e1d36e918d25 |
|---|
| 출처 메모 | uspto-grants-2001_10 |
|---|