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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197581Generated: November 2, 2026

Trityl chloride → 5-(4'-Methyl-(1,1'-biphenyl)-2-yl)-1-trityl-1H-tetrazole

https://huagongshe.com/reaction/1197581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantHCID 14425662HCID 14425662—
SolventPyridineHCID 1049—
Product5-(4'-Methyl-(1,1'-biphenyl)-2-yl)-1-trityl-1H-tetrazoleHCID 10152019—

Reaction Steps

A mixture of N-trimethylstannyl-5-(4'-methylbiphenyl-2-yl)tetrazole (Example 10, 0.4 g) and anhydrous pyridine (10 mL) was treated with triphenylmethyl chloride (0.3 g) and stirred at room temperature under a nitrogen atmosphere for 48 hours. The resulting solution was evaporated and the residue was partitioned between dichloromethane and saturated aqueous CuSO4. The organic layer was dried over MgSO4 and evaporated. The residual solid was triturated with diisopropyl ether and collected by filtration to give the title compound, mp 163°-165° C. (decomp., gas evol.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05276048
Source datasetuspto-grants-1994_01
ORD IDord-8474b7c0bc7245359223ea256ee909d7
Source noteuspto-grants-1994_01