HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299749Generated: October 29, 2026
Tetrahydrofuran → 4-(Tert-butyldimethylsilyloxy)benzyloxyamine
https://huagongshe.com/reaction/2299749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | N-[4-(tert-butyldimethylsilyloxy)benzyloxy]phthalimide | HCID 11825150 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(Tert-butyldimethylsilyloxy)benzyloxyamine | HCID 11821117 | 95.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06495581B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-89881f9db590407d98a9ce1cf7ffdc4c |
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| Source note | uspto-grants-2002_12 |
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