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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586813Generated: October 30, 2026

O-Xylene → 4-bromo-1-(4-tert-butyldiphenylsilyloxymethylphenyl)-2-(1-trityl-1H-tetrazol-5-yl)pyrrole

https://huagongshe.com/reaction/1586813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-XyleneHCID 7237—
ReactantAzido(trimethyl)stannaneHCID 5104973—
Reactant4-Bromo-1-(4-tert-butyldiphenylsilyloxymethylphenyl)pyrrole-2-carbonitrileHCID 19759559—
Product4-bromo-1-(4-tert-butyldiphenylsilyloxymethylphenyl)-2-(1-trityl-1H-tetrazol-5-yl)pyrroleHCID 19759467—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 4-bromo-1-(4-tert-butyldiphenylsilyloxymethylphenyl)pyrrole-2-carbonitrile (2.02 g) and trimethyltin azide (2.42 g) in xylene (20 ml) was stirred at 120° C. for 14 hours. After cooled to ambient temperature, the reaction mixture was concentrated in vacuo. To the residue was added trityl chloride (42 mg), triethylamine (50 μl) and methylene chloride (1 ml), and the mixture was treated in a conventional manner to give 4-bromo-1-(4-tert-butyldiphenylsilyloxymethylphenyl)-2-(1-trityl-1H-tetrazol-5-yl)pyrrole (1.63 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05215994
Source datasetuspto-grants-1993_06
ORD IDord-8a226c2ffee545b0b9679f04133daa7b
Source noteuspto-grants-1993_06