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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299749Generated: October 29, 2026

Tetrahydrofuran → 4-(Tert-butyldimethylsilyloxy)benzyloxyamine

https://huagongshe.com/reaction/2299749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium CarbonateHCID 11430—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantN-[4-(tert-butyldimethylsilyloxy)benzyloxy]phthalimideHCID 11825150—
SolventEthanolHCID 702—
Product4-(Tert-butyldimethylsilyloxy)benzyloxyamineHCID 1182111795.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

Hydrazine monohydrate (1.25 ml) was added to a solution of N-[4-(tert-butyldimethylsilyloxy)benzyloxy]phthalimide (5.00 g) in ethanol (10 ml)-tetrahydrofuran (40 ml) and stirred at 60° C. for 1 hour. 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 to obtain 4-(tert-butyldimethylsilyloxy)benzyloxyamine (3.15 g, yield 95%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495581B1
Source datasetuspto-grants-2002_12
ORD IDord-89881f9db590407d98a9ce1cf7ffdc4c
Source noteuspto-grants-2002_12