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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256347Generated: October 29, 2026

HCID 13961715, compound → HCID 178493575, compound

https://huagongshe.com/reaction/256347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13961715HCID 13961715—
ReactantHCID 178509299HCID 178509299—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178493575HCID 178493575—

Reaction Steps

A mixture of 0.90 g (0.0034 mole) of 3-methoxy-5-phenyl-2-benzofurancarboxylic acid and 0.55 g (0.0034 mole) of 1,1-carbonylbis(1H-imidazole) in 25 ml of tetrahydrofuran is stirred at reflux for one hour. To the mixture is added 0.29 g (0.0034 mole) of anhydrous 5-aminotetrazole, and the new mixture is stirred at reflux for an additional 16 hours. Cooling to room temperature results in precipitation of 3-methoxy-5-phenyl-N- 1H-tetrazol-5-yl-2-benzofurancarboxamide. The precipitate is filtered and recrystallized from methanol to yield 0.90 g 80% yield) of analytically pure tetrazole, mp 260°-262° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04703053
Source datasetuspto-grants-1987_10
ORD IDord-62f2d69d5b034f1792dd830d4a3cbd46
Source noteuspto-grants-1987_10