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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070049Generated: October 25, 2026

Tetrahydrofuran → 4-(5-Methyl-2-phenyl4-oxazolylmethoxy)benzyloxyamine

https://huagongshe.com/reaction/1070049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantN-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]phthalimideHCID 22344648—
SolventEthanolHCID 702—
SolventPotassium CarbonateHCID 11430—
Product4-(5-Methyl-2-phenyl4-oxazolylmethoxy)benzyloxyamineHCID 2234459390.3%

Reaction Steps

Hydrazine monohydrate (1.15 ml) was added to a solution of N-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]phthalimide (5.22 g) in ethanol (40 ml)-tetrahydrofuran (40 ml) and heated under reflux for 3 hours. The reaction mixture was cooled to room temperature, diluted with an aqueous solution of potassium carbonate and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The remaining crystals were recrystallized from ethyl acetate-hexane to obtain 4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine (3.32 g, yield 90%) as colorless crystals. m.p. 68-69° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251926B1
Source datasetuspto-grants-2001_06
ORD IDord-0087cbf933ca41bf99a09d9c24db27d1
Source noteuspto-grants-2001_06