Condense the Grignard reagent with a suitable carbonyl compound (e.g., a ketone or aldehyde) to form a diarylmethane intermediate. This can be achieved through a reaction with the carbonyl compound.
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N-(2-hydroxy-1,1-dimethylethyl)-5-chloro-2-fluorobenzamide
Thiourea, N-(2-methyl-4-oxo-3(4H)-quinazolinyl)-N'-(3-methylphenyl)-
4,5-Dimethyl-3-hydroxy-2,5-dihydrofuran-2-one
2-(4-(trifluoromethyl)phenyl)-6-methoxyquinoline
(5-(4-amino-6,7-dimethoxyquinazolin-2-ylamino)-2-hydroxyphenyl)-N,N,N-trimethylmethanaminium iodide
2-[(E)-2-phenylethenyl]-1-[(E)-3-phenylprop-2-en-1-yl]-1H-benzimidazole
2-[(E)-2-phenylethenyl]-1-[(E)-3-phenylprop-2-en-1-yl]-1H-benzimidazole
7-(phenoxathiin-2-yl)-9-phenyl-1,3,3a,5,6-pentaazacyclopenta[a]naphthalene-2-carboxylic acid
Chloroacetyl chloride
Benzaldehyde
5-(furan-2-yl)-8-phenyl-10-(trifluoromethyl)-2,3-dihydroimidazo[1,2-c]quinazoline-7-carboxamide
dipotassium tetrachloroplatinate
TETRAMETHYLTIN
carbon monoxide
C35H40N2O6
C17H16ClNO2
1,2-Bis(nonaflyl)benzene
THIOGLYCOLIC ACID N-BUTYL ESTER
5,7-DIMETHOXY-4-PROPYL-CHROMEN-2-ONE
1-(diethoxyphosphoryl)-2-(1-phenylethylidene)hydrazine
ethyl α-(3,4-dimethoxyphenyl)benzoylacetate
N,N,3,3-tetramethyl-1-(6-phenylpyridin-2-yl)butanamine
