42100-72-1Relevant academic research and scientific papers
Organohalide-catalyzed dehydrative O-alkylation between alcohols: A facile etherification method for aliphatic ether synthesis
Xu, Qing,Xie, Huamei,Chen, Pingliang,Yu, Lei,Chen, Jianhui,Hu, Xingen
supporting information, p. 2774 - 2779 (2015/05/27)
Organohalides are found to be effective catalysts for dehydrative O-alkylation reactions between alcohols, providing selective, practical, green, and easily scalable homo- and cross-etherification methods for the preparation of useful symmetrical and unsymmetrical aliphatic ethers from the readily available alcohols. Mechanistic studies revealed that organohalides are regenerated as reactive intermediates and recycled to catalyze the reactions.
Copper(II) bromide as efficient catalyst for silyl- to bisarylmethyl ethers interconversion (transprotection)
Specklin, Simon,Gallier, Florian,Mezaache, Rofia,Harkat, Hassina,Dembelé, Yénimégué Albert,Weibel, Jean-Marc,Blanc, Aurélien,Pale, Patrick
experimental part, p. 5820 - 5823 (2011/12/03)
Primary and secondary silylated alcohols are easily converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr2 as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.
Nafion-catalyzed preparation of benzhydryl ethers
Stanescu, Marina A,Varma, Rajender S
, p. 7307 - 7309 (2007/10/03)
Nafion-H is found to be an efficient and recyclable catalyst for the preparation of diphenylmethyl ethers of alcohols.
Iron-catalyzed solvent-free conversion of alcohols and phenols into diphenylmethyl (DPM) ethers
Namboodiri, Vasudevan V,Varma, Rajender S
, p. 4593 - 4595 (2007/10/03)
A catalytic amount of iron salts enables the solvent-free preparation of diphenylmethyl (DPM) ethers of alcohols and phenols at moderate temperatures.
