戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2285836作成日:2026年10月27日

Dibenzyl ether → Isobutyl ether

https://huagongshe.com/reaction/2285836

反応式

関与物質

役割名称HCID仕込み量
反応物Dibenzyl etherHCID 7657—
反応物3-Hydroxy-2,2-dimethylpropionaldehydeHCID 11699—
反応物Tetraaluminum;trisilicateHCID 21981400—
生成物Isobutyl etherHCID 12346—

反応手順

This isomerization reaction has been examined to a very large extent with regard to its mechanism and action of catalysts (J.Amer.Chem.Soc. 84, 3307 (1962)) and it was found that acidic catalysts are required for an isomerization and that of a great number of substances tested only silica gel and aluminum silicate in the form of pumice may practically be used as catalysts. But the activity and selectivity of these catalysts are not yet satisfactory from the economical point of view. Thus, the benzyl ether of hydroxypivalaldehyde can be prepared in the most favorable case with pumice with a conversion of 90 molar % and a selectivity of 83.3 molar %, i.e. a yield of 75 molar %. For the 2-methylpropyl ether, the yield with the same catalyst is 69 molar %, with a conversion of 84 molar % and a selectivity of 82.1 molar %, whereas the methyl ether is formed only in a yield of 38 molar %. When SiO2 is used as catalyst instead of pumice, the yield of the benzyl ether is even markedly lower, i.e. 46 molar %.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04324921
出典データセットuspto-grants-1982_04
ORD IDord-75bfd3df712047b6be3dc82b394e34ef
出典メモuspto-grants-1982_04