HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016179Generated: October 25, 2026
Potassium Carbonate → 1-(benzyloxymethyl)-2H-tetrazole
https://huagongshe.com/reaction/1016179
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzyl chloromethyl ether | HCID 137983 | — |
| Reactant | HCID 178418441 | HCID 178418441 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-((benzyloxy)methyl)-2H-tetrazole | HCID 10726340 | 44% |
| Product | 1-(benzyloxymethyl)-2H-tetrazole | HCID 67299845 | 47% |
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 overnight. The mixture was filtered, and the filtrate was concentrated in-vacuo. 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. 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985861B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-9e3632809eb14d998e770946a3548e0d |
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| Source note | uspto-grants-2011_07 |
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