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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2285836Generated: October 26, 2026

Dibenzyl ether → Isobutyl ether

https://huagongshe.com/reaction/2285836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenzyl etherHCID 7657—
Reactant3-Hydroxy-2,2-dimethylpropionaldehydeHCID 11699—
ReactantTetraaluminum;trisilicateHCID 21981400—
ProductIsobutyl etherHCID 12346—

Reaction Steps

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 %.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04324921
Source datasetuspto-grants-1982_04
ORD IDord-75bfd3df712047b6be3dc82b394e34ef
Source noteuspto-grants-1982_04