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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25480생성일: 2026년 10월 23일

Toluene → methyl (Z)-2-(2-oxotetrahydro-1H-1-pyrrolyl)-2-butenoate

https://huagongshe.com/ko/reaction/25480

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물2-PyrrolidoneHCID 12025—
반응물Phosphorus oxychlorideHCID 24813—
반응물2-Ketobutyric acid methyl esterHCID 545127—
용매WaterHCID 962—
생성물methyl (Z)-2-(2-oxotetrahydro-1H-1-pyrrolyl)-2-butenoateHCID 5907625760%

반응 단계

A 100 ml flask fitted with a magnetic stirring bar and a Dean-Stark trap was charged with methyl 2-oxobutanoate (7.5 g, 73 mmol), toluene (50 ml, 7 vol) and 2-pyrrolidinone (8.4 ml, 111 mmol, 1.5 equiv) followed by dropwise addition of POCl3 (1.6 ml, 20 mmol. 0.27 equiv). The reaction mixture was stirred under reflux with azeotropic removal of water via the Dean-Stark trap for 8 hours. After cooling down the solution was washed with 10% aq KHSO4 (2×3 vol). The aqueous phase was saturated with NaCl and back extracted with toluene (1×6 vol). The combined organic phase was dried over MgSO4, filtered and concentrated in vacuo to afford crude material (7.5 g) as an orange mobile oil. The crude oil was distilled (92-94° C., 0. 1 mm Hg) and gave pure product (4.7 g, 60%) as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858740B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-a072b4a0b2ab4c13ae93d6fccc95078a
출처 메모uspto-grants-2005_02