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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 355239생성일: 2026년 10월 24일

Triethylamine → (1R,2R)-ethyl 2-((methylsulfonyloxy)methyl)cyclopropanecarboxylate

https://huagongshe.com/ko/reaction/355239

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Ethyl (1R,2R)-2-(hydroxymethyl)cyclopropanecarboxylateHCID 29920784—
용매TetrahydrofuranHCID 8028—
생성물(1R,2R)-ethyl 2-((methylsulfonyloxy)methyl)cyclopropanecarboxylateHCID 53825740—

반응 조건

온도0 °C

반응 단계

A solution of trans-ethyl 2-hydroxymethyl-1-cyclopropanecarboxylate (1.136 g, 7.88 mmol) in dry tetrahydrofuran (20 ml) was cooled to 0° C. (ice bath), treated dropwise with mesyl chloride (0.675 ml, 8.66 mmol) and then treated immediately with triethylamine (1.32 ml, 9.52 mmol). This solution was stirred at 0° C. for 1.5 h (tlc indicated no substrate left). After dilution with ether (200 ml), the solution was washed with water, saturated ammonium chloride (10 ml), brine and dried over anhydrous magnesium sulfate. Evaporation of the solvent under reduced pressure gave a clear oil, 1.690 g (97%) which was used as such for the next step without purification. ir (film) νmax : 1720 cm-1 (C=O); 1Hmr (CDCl3) δ: 4.13 (2H, q, J=7, CH2 --CH3, 3.05 (2H, s, CH2 --OMs), 2.0~0.6 (4H, m, cyclopropyl), 1.27 ppm (3H, t, J=7, CH3 --CH2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04378314
출처 데이터셋uspto-grants-1983_03
ORD IDord-41c9eeaee4d84aefa6df148d6cab7119
출처 메모uspto-grants-1983_03