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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1264539생성일: 2026년 10월 24일

2,4,6-Trimethylpyridine → Methanesulfonic acid 2-(2-chloromethyl-phenyl)-ethyl ester

https://huagongshe.com/ko/reaction/1264539

반응식

참여 물질

역할이름HCID투입량
반응물2,4,6-TrimethylpyridineHCID 7953—
반응물Methanesulfonyl chlorideHCID 31297—
반응물2-[2-(Hydroxymethyl)phenyl]ethanolHCID 239024—
반응물Lithium ChlorideHCID 433294—
용매DimethylformamideHCID 6228—
생성물Methanesulfonic acid 2-(2-chloromethyl-phenyl)-ethyl esterHCID 5432882645%

반응 조건

온도0 °C

반응 단계

Mix 2-(2-hydroxymethyl-phenyl)-ethanol (12.0 g, 78.8 mmol) and collidine (23 mL, 0.17 mol) and treat with lithium chloride (7.35 g, 0.173 mmol) in dimethylformamide (125 mL). Cool in an ice bath and treat, by dropwise addition, with mesyl chloride (13.4 mL). Stir at 0° C. for 4 hours, partition between ice water (300 mL) and a 1:1 mixture of ether:pentane (2×400 mL). Wash the organic layer with a saturated solution of CuSO4 (2×200 mL), dry (MgSO4) and purify by silica gel chromatography (2.5:1 hexane/ethyl acetate followed by 2:1 hexane/ethyl acetate followed by 3:2 hexane/ethyl acetate) to give methanesulfonic acid 2-(2-chloromethyl-phenyl)-ethyl ester as a pale yellow oil (8.8 g, 45%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06544980B2
출처 데이터셋uspto-grants-2003_04
ORD IDord-acf7392e4e924400b8265eaf73daafc3
출처 메모uspto-grants-2003_04