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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070075Generated: October 30, 2026

Tetrahydrofuran → 4-(Tert-butyldimethylsilyloxy)benzyloxyamine

https://huagongshe.com/reaction/1070075

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 numberUS06251926B1
Source datasetuspto-grants-2001_06
ORD IDord-500ebdcb90ea4f3fb71f5e4387993764
Source noteuspto-grants-2001_06