돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1680337생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1680337

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 번호US04272437
출처 데이터셋uspto-grants-1981_06
ORD IDord-a98069384f194f889f0a923993f1e4d1
출처 메모uspto-grants-1981_06