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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888108Generated: October 25, 2026

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

https://huagongshe.com/reaction/1888108

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 mixture was stirred for 4 hours. Analysis by LC/MS indicated that the reaction was not complete, so the reaction was treated with benzyl chloromethyl ether (0.5 g, 3.19 mmol) and stirred for about 16 h. After this time, 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 concentrated in vacuo to yield a residue. The residue was purified over a 6×20 mm silica gel column, eluting with 20% then 30% ethyl acetate/hexanes to yield the title compound (2.39 g, 44% yield), and 1-(benzyloxymethyl)-2H-tetrazole (2.56 g, 47% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501782B2
Source datasetuspto-grants-2013_08
ORD IDord-2048772766ec48038c53957ace20d300
Source noteuspto-grants-2013_08