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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1195381Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1195381

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon TetrachlorideHCID 5943—
EduktTetrahydrofuranHCID 8028—
Edukt4,4'-DifluorobenzophenoneHCID 9582—
EduktEthyl(1-methyl-1h-tetrazol-5-yl)acetateHCID 283414—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelWaterHCID 962—
LösungsmittelPyridineHCID 1049—
ProduktEthyl 3,3-bis(4-fluorophenyl)-2-(1-methyl-1H-tetrazol-5-yl)-2-propenoateHCID 14539522—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05110940
Quelldatensatzuspto-grants-1992_05
ORD IDord-7a00494d288e44e9bb160e5d92803f7b
Quellennotizuspto-grants-1992_05