Bulletin of the Chemical Society of Japan p. 2585 - 2588 (1989)
Update date:2022-08-11
Topics:
Kajigaeshi, Shoji
Kawamukai, Hiroshi
Fujisaki, Shizuo
The reaction of primary alcohols or simple ethers and α,ω-diols or cyclic ethers with a stoichiometric amount of benzyltrimethylammonium tribromide (BTMA) Br3) in carbon tetrachloride in the presence of Na2HPO4 aq or in acetic acid in the presence of CH3CO2Na aq at 60-70 deg C gave dimeric esters and lactones respectively in good yields.The reaction of secondary alcohols with 1 equiv of BTMA Br3 in the presence of a buffer at 60 deg C gave ketones.
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