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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 261952생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/261952

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물1-VinylimidazoleHCID 66171—
반응물(2-tert-Butylphenyl)(phenyl)methanoneHCID 54101900—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물alpha-(o-Tert.-butylphenyl)-alpha-phenyl-1-vinylimidazole-2-methanolHCID 12433926—

반응 조건

온도-60 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04152441
출처 데이터셋uspto-grants-1979_05
ORD IDord-6d2feb51346041a8ac3d69a3a8266c78
출처 메모uspto-grants-1979_05