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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33275생성일: 2026년 10월 27일

Hydrochloric Acid → 4-(2,2,2-Trifluoro-ethoxy)-1H-pyrazole-3,5-dicarboxylic acid diethyl ester

https://huagongshe.com/reaction/33275

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물1,10-PhenanthrolineHCID 1318—
반응물2,2,2-TrifluoroethanolHCID 6409—
반응물3,5-diethyl 4-iodo-1H-pyrazole-3,5-dicarboxylateHCID 11739230—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매EthanolHCID 702—
생성물4-(2,2,2-Trifluoro-ethoxy)-1H-pyrazole-3,5-dicarboxylic acid diethyl esterHCID 57474425—

반응 단계

To a solution of 1 g 4-Iodo-1H-pyrazole-3,5-dicarboxylic acid diethyl ester in 5 ml 2,2,2-trifluoro-ethanol 1.4 g Cs2CO3, 56 mg CuI and 106 mg 1,10-Phenanthroline were added. The reaction mixture heated for 4 h to 100° C. under microwave irradiation (100 W, CEM Discover™ apparatus). Then 10 HCl in ethanol (8M) was added and the solution was stirred at RT. After 16 h the solvents were removed under reduced pressure and the residue taken up in DCM and water. The organic phase was separated and the aqueous layer was extracted with DCM (2×50 ml). The combined organic layers were dried over MgSO4, filtered and the solvent was removed under reduced pressure. The residue was purified by preparative HPLC (C18 reverse phase column, elution with a H2O/MeCN gradient with 0.1% TFA). The fractions containing the product were evaporated and lyophilized to yield a white solid. Yield: 359 mg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429581B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-f62670b42552435cbab75bf3e1bab8a4
출처 메모uspto-grants-2008_09