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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1195381생성일: 2026년 10월 26일

Carbon Tetrachloride → Ethyl 3,3-bis(4-fluorophenyl)-2-(1-methyl-1H-tetrazol-5-yl)-2-propenoate

https://huagongshe.com/reaction/1195381

반응식

참여 물질

역할이름HCID투입량
반응물Carbon TetrachlorideHCID 5943—
반응물TetrahydrofuranHCID 8028—
반응물4,4'-DifluorobenzophenoneHCID 9582—
반응물Ethyl(1-methyl-1h-tetrazol-5-yl)acetateHCID 283414—
촉매Titanium TetrachlorideHCID 24193—
용매WaterHCID 962—
용매PyridineHCID 1049—
생성물Ethyl 3,3-bis(4-fluorophenyl)-2-(1-methyl-1H-tetrazol-5-yl)-2-propenoateHCID 14539522—

반응 조건

온도0 °C

반응 단계

A mixture of titanium tetrachloride (2 mL) and carbon tetrachloride (2 mL) was added to 15 mL of tetrahydrofuran at -78° C. under an argon atmosphere. The suspension was stirred at -78° C. for 30 minutes before 0.2 g of 4,4'-difluorobenzophenone was added. After stirring for an additional 30 minutes, a solution of 0.15 g of ethyl 1-methyl-5-tetrazolylacetate in 1 mL of dry pyridine was added dropwise. The dark brownish suspension was stirred at -78° C. for 15 minutes, then was allowed to warm to 0° C. forming a thick paste. The mixture was allowed to stand for 24 hours at ambient temperature before it was poured into water. The aqueous mixture was extracted with ethyl acetate to yield crude product. Analytical TLC eluted five times with 20% (v/v) ethyl acetate in hexanes showed the desired product at Rf =0.3. Purification by preparative chromatography on two 20×20 cm2 0.25 mm TLC plates eluted twice with 20% (v/v) ethyl acetate in hexanes to give the title compound which was identical to the compound of Example 3, Step A.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05110940
출처 데이터셋uspto-grants-1992_05
ORD IDord-7a00494d288e44e9bb160e5d92803f7b
출처 메모uspto-grants-1992_05