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HRID 330682作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/330682

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon TetrachlorideHCID 5943—
反応物TetrahydrofuranHCID 8028—
反応物4,4'-DifluorobenzophenoneHCID 9582—
反応物Ethyl(1-methyl-1h-tetrazol-5-yl)acetateHCID 283414—
触媒Titanium TetrachlorideHCID 24193—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
生成物Ethyl 3,3-bis(4-fluorophenyl)-2-(1-methyl-1H-tetrazol-5-yl)-2-propenoateHCID 14539522—

反応条件

温度0 °C

反応手順

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. Pruification by preparative chromatography on two 20×20 cm 2 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04897490
出典データセットuspto-grants-1990_01
ORD IDord-b3c777ff545449c0860d8d3fdfc7e356
出典メモuspto-grants-1990_01