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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 337587생성일: 2026년 10월 25일

Dichloromethane → 2-[3,4-Dichloro-5-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)phenyl]ethyl methanesulfonate

https://huagongshe.com/reaction/337587

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Methanesulfonyl chlorideHCID 31297—
반응물DiisopropylethylamineHCID 81531—
반응물2-[3,4-Dichloro-5-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)phenyl]ethanolHCID 66895403—
용매Diethyl EtherHCID 3283—
생성물2-[3,4-Dichloro-5-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)phenyl]ethyl methanesulfonateHCID 86651668—

반응 조건

온도0 °C

반응 단계

To a dichloromethane (0.11 M) solution of 2-[3,4-dichloro-5-({[(1,1-dimethylethyl)(dimethyl)silyl]oxy}methyl)phenyl]ethanol (1 eq.) from the previous step was added at 0° C. Hunig's base (1.5 eq.) and methanesulfonyl chloride (1.1 eq.). The resulting suspension was stirred at 0° C. for 30 min and at RT for 15 min. The reaction was then diluted with ether and quenched with 1N aq. HCl. The aqueous layer was separated and back-extracted with ether. The combined organic extracts were washed further with 1 N aq. NaOH, water and brine, dried over Na2SO4, filtered and the filtrate concentrated in vacuo to give the title compound as a brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889714B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-ba30d19d5c82457cabbcda5757a1e3a4
출처 메모uspto-grants-2014_11