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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54619생성일: 2026년 10월 26일

Methyl iodide → 2-Methyl 1-(phenylmethyl) (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylate

https://huagongshe.com/reaction/54619

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Cesium carbonateHCID 10796—
반응물1-(Phenylmethyl) (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylateHCID 391517—
용매MethanolHCID 887—
생성물2-Methyl 1-(phenylmethyl) (2S,4R)-4-hydroxy-1,2-pyrrolidinedicarboxylateHCID 688411—

반응 단계

A solution of N-benzyloxycarbonyl-4-hydroxy-L-trans-proline 9 (47.5 g; 179 mmol) in anhydrous methanol (900 ml) is adjusted to pH=9.0-9.5 using caesium carbonate. The mixture is subsequently stirred at room temperature for 30 min., and then concentrated. After having been dried for 30 minutes under high vacuum, the residue is taken up in anhydrous N,N-dimethylformamide (900 ml). Iodomethane (28.0 g; 197 mmol) is added, and the mixture is stirred at room temperature for 21 h. The solution is concentrated, and the residue is subsequently distilled repeatedly with toluene, taken up in chloroform (1.8 l), and then extracted by shaking once with each of water and a 10% solution of sodium hydrogen carbonate, and once again with water (600 ml on each occasion). The organic phase is dried (magnesium sulphate) and concentrated. Yield: 50.0 g (quantitative).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05623049
출처 데이터셋uspto-grants-1997_04
ORD IDord-b35c38b9ff214bfca75dac9a92614f14
출처 메모uspto-grants-1997_04