Methyl Benzoate Infrared Spectrum

The intermediate cyclooctene complex appears to be more reactive with respect to CS coordination and more sensitive to oxidation when the arene ring bears electron-withdrawing groups (e.g., C02CH3). Dicarbonyl(methyl rj6-benzoate)-thiocarbonyl)chromium is air stable in the solid state and reasonably stable in solution.9 The infrared spectrum exhibits metal carbonyl absorptions at 1980 and 1935 cm"1 and a metal thiocarbonyl stretch at 1215 cm"1 (Nujol) (these occur at 1978, 1932, and 1912 cm"1 in CH2C12 solution).10 Irradiation of the compound in the presence of phosphite or phosphine leads to slow substitution of CO by these ligands, whereas the CS ligand remains inert to substitution. The crystal structure has been published."... 

The reactions of the isomeric dimethylpyrazines and trimethyl-pyrazine with methyllithium have been studied in order to gain insight into the factors involved in the competition between ring methylation and side-chain metalation.189 The major product from the reaction of 2,5-dimethylpyrazine and ethereal methyllithium was shown to be trimethylpyrazine, thus confirming Klein and Spoerri s earlier observation.190,191 Tetramethylpyrazine was also formed as a by-product. Proof of side-chain metalation was obtained by treatment of the reaction mixture with methyl benzoate and isolation of 2-methyl-5-phenacylpyrazine. Evidence for the presence of dihydro-and tetrahydropyrazine intermediates is derived from the infrared spectrum of the crude product obtained on hydrolysis of the reaction mixture which shows C=N and N-H absorptions (see Scheme 17). 

Infrared spectrum of methyl benzoate (neat liquid, salt plates). 

---