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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299724Generated: October 25, 2026

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

https://huagongshe.com/reaction/2299724

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 numberUS06495581B1
Source datasetuspto-grants-2002_12
ORD IDord-15a7b399b44543549e306d01d36d3bd2
Source noteuspto-grants-2002_12