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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1689485생성일: 2026년 10월 26일

Triethylamine → 2-(4-Formylphenoxy)ethyl methanesulfonate

https://huagongshe.com/reaction/1689485

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Benzaldehyde, 4-(2-hydroxyethoxy)-HCID 89178—
용매DichloromethaneHCID 6344—
생성물2-(4-Formylphenoxy)ethyl methanesulfonateHCID 22288650—

반응 조건

온도0 °C

반응 단계

Methanesulfonylchloride (3.3 mL) was added dropwise over 5 min to a solution of 4-(2-hydroxyethoxy)benzaldehyde (example 108, step a) (6.4 g) and triethylamine (6.4 mL) in DCM (30 mL) at 0° C. under argon. The resulting mixture was stirred at 0° C. for 10 min and then at RT for 1 h. The reaction mixture was washed with brine (2×30 mL), dried over sodium sulphate, filtered and evaporated in vacuo. The residue was purified by silica gel chromatography eluting with 40-50% EtOAc in petroleum ether (40-60° C.) to give the subtitled compound as a viscous yellow oil. Yield 8.87 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08148373B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-06a15d1e0f5d46a3847ad9b3d9ba2f12
출처 메모uspto-grants-2012_04