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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 637042생성일: 2026년 10월 26일

Methanesulfonyl chloride → 3,4,5-Trimethoxybenzyl Mesylate

https://huagongshe.com/reaction/637042

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물3,4,5-Trimethoxybenzyl alcoholHCID 77449—
반응물DiisopropylethylamineHCID 81531—
용매AcetonitrileHCID 6342—
생성물3,4,5-Trimethoxybenzyl MesylateHCID 18464591—

반응 단계

Combine 3,4,5-trimethoxybenzyl alcohol (9.0 g, 45.4 mmol), N,N-diisopropylethylamine (12.9 g, 100 mmol), and acetonitrile (60 mL). Cool in an ice bath. Add methanesulfonyl chloride (6.76 g, 49.0 mmol). After 2 hours, partition the reaction mixture between water and ethyl acetate. Separate the layers and extract the organic layer with 1 M hydrochloric acid solution and them a saturated solution of sodium bicarbonate. Dry the organic layer over Na2SO4, filter, and evaporate in vacuo to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06194406B1
출처 데이터셋uspto-grants-2001_02
ORD IDord-29826fabea994dc48c092b20a9be0cd1
출처 메모uspto-grants-2001_02