Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 480078생성일: 2026년 10월 26일
(+-)-Penicillamine → 2-Amino-3-methyl-3-((2,4,6-trimethoxyphenyl)methylthio)butanoic acid
https://huagongshe.com/reaction/480078
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (+-)-Penicillamine | HCID 4727 | — |
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | 2,4,6-Trimethoxybenzyl alcohol | HCID 602515 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-Amino-3-methyl-3-((2,4,6-trimethoxyphenyl)methylthio)butanoic acid | HCID 23508365 | 95% |
반응 단계
A suspension of 2-amino-3-methyl-3-sulfanylbutanoic acid (D-penicillamine) (5.0 g, 34 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. Then 2,4,6-trimethoxy-benzyl alcohol (6.64 g, 34 mmol) in CH2Cl2 (137 mL) was added dropwise at 0° C. with stirring. Stirring was continued for 1 hour at 0° C. and then for 2 hours at room temperature. The solvent was removed in vacuo 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. 1H-NMR (300 MHz, CDCl3) δ 6.10 (s, 2H), 3.84 (s, 6H), 3.76 (s, 3H), 3.40-4.10 (m, 3H), 1.69 (s, 3H), 1.23 (s, 3H); mass spectrum (API-TIS) m/z 330 (MH+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06649629B2 |
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| 출처 데이터셋 | uspto-grants-2003_11 |
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| ORD ID | ord-5f9081e52a454fd78bd251a34444683b |
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| 출처 메모 | uspto-grants-2003_11 |
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