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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580944Generated: October 30, 2026

1-(4-Benzyloxy-phenyl)-5-trifluoromethyl-1H-tetrazole → 4-(5-Trifluoromethyl-tetrazol-1-YL)-phenol

https://huagongshe.com/reaction/580944

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Benzyloxy-phenyl)-5-trifluoromethyl-1H-tetrazoleHCID 21197251—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product4-(5-Trifluoromethyl-tetrazol-1-YL)-phenolHCID 2119724999.8%

Reaction Steps

A solution of 1-(4-benzyloxy-phenyl)-5-trifluoromethyl-1H-tetrazole (45.3 mmol) in ethanol (100 ml) and tetrahydrofuran (100 ml) was hydrogenated at room temperature and atmospheric pressure over 10% palladium-carbon catalyst (6 g). After 2 h, the mixture was filtered and the filtrate was evaporated to give the title compound (10.4 g) as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05919803
Source datasetuspto-grants-1999_07
ORD IDord-00c47597b25a4338804bc7f64acfbad4
Source noteuspto-grants-1999_07