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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261952Generated: October 26, 2026

Carbon Dioxide → alpha-(o-Tert.-butylphenyl)-alpha-phenyl-1-vinylimidazole-2-methanol

https://huagongshe.com/reaction/261952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant1-VinylimidazoleHCID 66171—
Reactant(2-tert-Butylphenyl)(phenyl)methanoneHCID 54101900—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Productalpha-(o-Tert.-butylphenyl)-alpha-phenyl-1-vinylimidazole-2-methanolHCID 12433926—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a solution of 28.8 g. (0.25 mol) of N,N,N',N'-tetramethylethylenediamine and 17.6 g. (0.19 mol) of 1-vinylimidazole in 300 ml. of anhydrous tetrahydrofuran, 14 ml. (0.25 mol) of 20% butyllithium in n-hexane were added drop-wise with stirring at -60° C., and under a nitrogen atmosphere over the course of one hour. Stirring was continued for 2 hours under the same conditions, after which a solution of 48 g. (0.20 mol) of 2-tert.-butylbenzophenone in 300 ml. of anhydrous tetrahydrofuran was added drop-wise. The reaction mixture was stirred for 3.5 hours, after which the cooling means was removed and stirring was continued overnight under the nitrogen atmosphere. The lithium complex obtained was then decomposed with 15 ml. of water and a large excess of solid carbon dioxide. The precipitate was filtered off, the filtrate was dried over sodium sulphate and the solvent was distilled off. The solid residue was twice crystallised from ethyl acetate to which a small amount of ethanol had been added. α-(o-tert.-Butylphenyl)-α-phenyl-1-vinylimidazole-2-methanol was obtained. Melting point 152°-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152441
Source datasetuspto-grants-1979_05
ORD IDord-6d2feb51346041a8ac3d69a3a8266c78
Source noteuspto-grants-1979_05