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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070060Generated: October 25, 2026

Tetrahydrofuran → 3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine

https://huagongshe.com/reaction/1070060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium CarbonateHCID 11430—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantN-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]phthalimideHCID 11732904—
SolventEthanolHCID 702—
Product3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamineHCID 1092494697%

Reaction Steps

Hydrazine monohydrate (0.661 ml) was added to a solution of N-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]phthalimide (3.00 g) in ethanol (25 ml)-tetrahydrofuran (25 ml) and heated under reflux for 3 hours. The reaction mixture was cooled to room temperature, an aqueous solution of potassium carbonate was added 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 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine (2.04 g, yield 97%) as pale-yellow crystals. m.p. 81-82° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251926B1
Source datasetuspto-grants-2001_06
ORD IDord-9cd42e1797b740298216b5ddeb00115d
Source noteuspto-grants-2001_06