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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 444565생성일: 2026년 10월 23일

Hydrochloric Acid → Ethyl 3-fluoro-4-cyclohexylphenylglyoxylate

https://huagongshe.com/ko/reaction/444565

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Boric AcidHCID 7628—
반응물Hydrofluoric AcidHCID 14917—
반응물Ethyl 3-amino-4-cyclohexylphenylglyoxylateHCID 20515218—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
생성물Ethyl 3-fluoro-4-cyclohexylphenylglyoxylateHCID 20515163—

반응 조건

온도0 °C

반응 단계

To 44.2 g. (0.15 moles) of ethyl 3-amino-4-cyclohexylphenylglyoxylate is added at 0° C. 44 ml. of 1.5 moles of concentrated hydrochloric acid. The reaction mixture is maintained at 0° C. and the diazonium salt is prepared with 23.2 g. (0.32 moles) of 95% sodium nitrite in 80 ml. of water. To this mixture is rapidly added a solution of 10.4 g. (0.17 moles) of boric acid dissolved in 22 g. (0.66 moles) of 60% hydrofluoric acid. The reaction mixture is then stirred for 1/2 hour and filtered, washed with 3×25 ml. of water, 2×25 ml. of methanol and 25 ml. of ether. The residual cake is then treated in vacuo. The treated cake is then placed in a distilling flask and heated to permit spontaneous decomposition. After the decomposition, the residue is then fractionally distilled to obtain ethyl 3-fluoro-4-cyclohexylphenylglyoxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04264627
출처 데이터셋uspto-grants-1981_04
ORD IDord-f170f5a146bd4d3dbcadab51e8a0dc8e
출처 메모uspto-grants-1981_04