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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42543Generated: October 25, 2026

Potassium Carbonate → 1-(benzyloxymethyl)-2H-tetrazole

https://huagongshe.com/reaction/42543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzyl chloromethyl etherHCID 137983—
ReactantHCID 178418441HCID 178418441—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2-((benzyloxy)methyl)-2H-tetrazoleHCID 1072634044%
Product1-(benzyloxymethyl)-2H-tetrazoleHCID 6729984547%

Reaction Steps

A suspension of 1-H-tetrazole (2.0 g, 28.5 mmol) and potassium carbonate (5.9 g, 42.7 mmol) in DMF (30 mL) was treated with benzyl chloromethyl ether (5.36 g, 34.2 mmol), and the reaction mixture was stirred for 4 hours. After this time, the reaction mixture was analyzed by LC/MS, which indicated that the reaction was not complete. As a result, the reaction was treated with benzyl chloromethyl ether (0.5 g, 3.19 mmol) and stirred for about 16 additional hours. At the conclusion of this period, the mixture was filtered, and the filtrate was concentrated in vacuo to yield a residue. The residue was diluted with diethyl ether (200 mL), washed 5× with water (50 mL), once with brine, dried over sodium sulfate, and then concentrated in vacuo. The resulting residue was purified over a 6×20 mm silica gel column, eluting with 20% then 30% ethyl acetate/hexanes to yield 2-(benzyloxymethyl)-2H-tetrazole (2.39 g, 44% yield) and 1-(benzyloxymethyl)-2H-tetrazole (2.56 g, 47% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536198B2
Source datasetuspto-grants-2013_09
ORD IDord-dbce395804984eb8bb043e9523eb5a17
Source noteuspto-grants-2013_09