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578703-90-9

1-(4-fluorophenyl)-1H-1,2,3-triazole-4-carbaldehyde synthesis

8synthesis methods
1H-1,2,3-Triazole-4-methanol, 1-(4-fluorophenyl)-

1225046-93-4
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1-(4-fluorophenyl)-1H-1,2,3-triazole-4-carbaldehyde

578703-90-9
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Yield:578703-90-9 79%

Reaction Conditions:

with Jones reagent in acetone at 0; for 0.583333 h;

Steps:

Preparation of 1- substituted-(1,2,3)triazol-4-carbaldehyde (3)

General procedure: 1-substituted-(1,2,3)triazol-4-yl-methanol 2 ( 4 mmol) was taken in dry acetone and cool to 0 0C and added the Jones reagent (CrO3+H2SO4+Acetone) (4 mmol) slowly over 15 mins. The reaction mixture was stirred for 20 mins at 0 0C. After completion of reaction, the reaction mixture was filtered through the short pad of celite and collected the filtrate, and concentrated under vaccum. The residue was purified by passing through a column packed with silica gel using petroleum ether/EtOAc (8:2) as eluents.

References:

Sambasiva Rao;Kurumurthy;Veeraswamy;Santhosh Kumar;Shanthan Rao;Pamanji;Venkateswara Rao;Narsaiah [Bioorganic and Medicinal Chemistry Letters,2013,vol. 23,# 5,p. 1225 - 1227] Location in patent:supporting information

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