32836-42-3

Upstream product

• 334-48-5 1-decanoic acid 
• 74-88-4 methyl iodide 
• 75-16-1 methylmagnesium bromide 
• 112-13-0 n-decanoyl chloride 

Downstream Products

• 100186-18-3 4-(1,1-Dimethyl-decyl)-benzene-1,2-diol 
• 56888-88-1 2-methyl-undec-2-ene 
• 18516-37-5 2-methyl-undec-1-ene 
• 163399-21-1 1,1-dimethyldecanyl acetate 
• 569332-34-9 2-(3,5-dimethoxy-4-hydroxyphenyl)-2-methylundecane 
• 1258870-44-8 C₂₄H₃₅ClOSi 
• 144381-57-7 sodium 5-<(1,1-dimethyl)decyl>-2-(oxymethyl-18-crown-6)methylbenzenephosphonate 
• 144381-56-6 sodium monoethyl 5-<(1,1-dimethyl)decyl>-2-(oxymethyl-15-crown-5)methylbenzenephosphonate 
• 144381-55-5 [2-Bromomethyl-5-(1,1-dimethyl-decyl)-phenyl]-phosphonic acid monoethyl ester 
• 144381-53-3 diethyl 5-<(1,1-dimethyl)decyl>-2-methylbenzenephosphonate 
• 144381-54-4 monoethyl 5-<(1,1-dimethyl)decyl>-2-methylbenzenephosphonate 
• 144381-52-2 4-<(1,1-dimethyl)decyl>-2-iodotoluene 
• 144381-51-1 4-<(1,1-dimethyl)decyl>toluene 
• 569332-38-3 5-(1,1-dimethyl-decyl)-benzene-1,3-diol 

Relevant academic research and scientific papers

A new synthetic method for methyl ketones from carboxylic acids using metallic strontium and methyl iodide

Carboxylic acids reacted with metallic strontium and methyl iodide to give methyl ketones preferentially in moderate to good yields. Copyright

Reactions of in situ formed acyl tributylphosphonium ions with Grignard reagents as an effective route to ketones from acid chlorides

The reactions of acyl tributylphosphonium ions in situ generated from acid chlorides and Bu3P in THF at -22°C with primary alkyl and arylmagnesium halides have proved to be a convenient and simple procedure to prepare ketones from acid chloride in one-pot.