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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 420015생성일: 2026년 10월 25일

Methyl 4-chloroformylbutyrate → 2-(5-methoxycarbonyl-2-oxopentylidene)-3-methyl-3H-benzothiazole

https://huagongshe.com/reaction/420015

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 4-chloroformylbutyrateHCID 73916—
반응물2,3-Dimethyl-6-sulfobenzothiazolium tosylateHCID 86585228—
용매PyridineHCID 1049—
생성물2-(5-methoxycarbonyl-2-oxopentylidene)-3-methyl-3H-benzothiazoleHCID 66651518—

반응 조건

온도55 °C

반응 단계

To 1.7 g of 2,3-dimethyl-6-sulfobenzothiazolium tosylate in 20 mL of pyridine at room temperature is added 1 mL of methyl 5-chloro-5-oxovalerate. The mixture is heated at 50-60° C. for 3 hours. The pyridine solvent is removed under reduced pressure, and the reaction is worked up with chloroform and brine, and purified by silica gel column to yield 0.5 g of 2-(5-methoxycarbonyl-2-oxopentylidene)-3-methyl-3H-benzothiazole. A mixture of 0.45 g of this benzothiazole and 0.45 g of phosphorous oxychloride in 5 mL of dichloroethane is heated at reflux for 2 hours to generate 2-(2-chloro-2-methoxycarbonylpropylvinyl)-3-methylbenzothiazolium chloride. The volatile components are evaporated and the crude chloride is used without further purification. The crude chloride and 0.5 g of Compound 12 is stirred in 5 mL of dichloroethane in the presence of 0.45 mL of triethylamine for 2 hours. The volatile components are removed under reduced pressure, and the residue is dissolved in 5 mL of methanol and added dropwise to a solution of 4.5 g of sodium iodide in 30 mL water. The sticky solid is purified by HPLC to yield Compound 37.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093411B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-d16c8c0c2b784ca7bd0db7f11d555c01
출처 메모uspto-grants-2012_01