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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423255Generated: October 25, 2026

Isopropyl iodide → 5-(4-Benzyloxyphenyl)-2-isopropyl-2H-tetrazole

https://huagongshe.com/reaction/423255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantSodium hydrideHCID 24758—
Reactant5-[4-(benzyloxy)phenyl]-2H-tetrazoleHCID 4770909—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product5-(4-Benzyloxyphenyl)-2-isopropyl-2H-tetrazoleHCID 5862978297.9%

Reaction Steps

5-(4-Benzyloxyphenyl)-2H-tetrazole (500 mg) was added to a suspension of sodium hydride (96 mg) in dimethylformamide (5 mL) under ice-cooling. The mixture was stirred at room temperature for 0.5 hour. After addition of isopropyl iodide (405 mg) thereto, the mixture was stirred at 60° C. for 2 hours under heating. The reaction mixture was allowed to stand for cooling down to room temperature, diluted with ethyl acetate, washed with water and saturated brine, dried anhydrous sodium sulfate, and concentrated. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=4:1, v/v) to give the title compound (571 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101774B2
Source datasetuspto-grants-2012_01
ORD IDord-f91d6be9cbca49738da14158e811620d
Source noteuspto-grants-2012_01