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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35460생성일: 2026년 10월 26일

Ethyl chloroformate → ethyl 2,3,4-trimethyl-l (4H)-pyridinecarboxylate

https://huagongshe.com/reaction/35460

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물2,3-LutidineHCID 11420—
반응물HCID 178418332HCID 178418332—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매TetrahydrofuranHCID 8028—
생성물ethyl 2,3,4-trimethyl-l (4H)-pyridinecarboxylateHCID 86742392—

반응 단계

A solution of 6.75 g of 2,3-lutidine and 475 mg of copper(I) iodide in 150 ml of abs. tetrahydrofuran is cooled to -20° and treated under argon with 3.4 ml of ethyl chloroformate. The reaction mixture is heated to 30° and treated dropwise within 10 minutes with 14 ml of methylmagnesium chloride (3 molar, in tetrahydrofuran). The ethyl 2,3,4-trimethyl-l (4H)-pyridinecarboxylate obtained as the intermediate can be isolated as follows: The reaction mixture is cooled to -10° and treated with 38 ml of aqueous (20%) ammonium chloride solution, whereupon 100 ml of ether are added and the organic solution is washed several times with a 20% ammonium chloride/ammonia (1:1) solution, 2N hydrochloric acid and 10% sodium carbonate solution. The organic solution is dried and concentrated, and the residue is purified on a silica gel column, the medium pressure flash chromatography method (solvent: n-hexane/ether [20:1]) being used and the pressure being produced with nitrogen gas.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04766133
출처 데이터셋uspto-grants-1988_08
ORD IDord-bc2024f6a43d4c4ea3d71242dd15c4d3
출처 메모uspto-grants-1988_08