2002Unpublished venueRequires access

Lmproving the Synthetic Process of 3,4,5-Trimethoxy Benzaldehyde

Feng Yang

Open publisher page 0 citations

Abstract

P hydroxy benzaldehyde reacts with bromine to form 3,5 bromo 4 hydroxy benzaldehyde,then fwthes reaction occurs with sodium methylate to obtain 3,5 methoxy 4 hydroxy benzaldehyde in the solution of DMF and employing cuprous chloride as catalyst.In the end,this compound is methylafed by bimethyl sulphade to synthesize 3,4,5 trimethoxy benzaldehyde at pH 10.

About this research paper

What this paper is about

P hydroxy benzaldehyde reacts with bromine to form 3,5 bromo 4 hydroxy benzaldehyde,then fwthes reaction occurs with sodium methylate to obtain 3,5 methoxy 4 hydroxy benzaldehyde in the solution of DMF and employing cuprous chloride as catalyst.In the end,this compound is methylafed by bimethyl sulphade to synthesize 3,4,5 trimethoxy benzaldehyde at pH 10.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

P hydroxy benzaldehyde reacts with bromine to form 3,5 bromo 4 hydroxy benzaldehyde,then fwthes reaction occurs with sodium methylate to obtain 3,5 methoxy 4 hydroxy benzaldehyde in the solution of DMF and employing cuprous chloride as catalyst.In the end,this compound is methylafed by bimethyl sulphade to synthesize 3,4,5 trimethoxy benzaldehyde at pH 10.

Key concepts: Benzaldehyde, Bromine, Chemistry, Organic chemistry, Catalysis

Related papers

Back to paper searchBrowse research topicsOriginal source
Lmproving the Synthetic Process of 3,4,5-Trimethoxy Benzaldehyde — Research Paper | ScholarLens