関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (+-)-Penicillamine | HCID 4727 | — |
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | 2,4,6-Trimethoxybenzyl alcohol | HCID 602515 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-Amino-3-methyl-3-((2,4,6-trimethoxyphenyl)methylthio)butanoic acid | HCID 23508365 | 95% |
反応手順
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+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06649629B2 |
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| 出典データセット | uspto-grants-2003_11 |
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| ORD ID | ord-5f9081e52a454fd78bd251a34444683b |
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| 出典メモ | uspto-grants-2003_11 |
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