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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301836Generated: October 26, 2026

5-(Tert-butyldimethylsilyloxy)-2-phthalimido-1-nitrobenzene → 5-(Tert-butyldimethylsilyloxy)-2-phthalimidoaniline

https://huagongshe.com/reaction/2301836

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Tert-butyldimethylsilyloxy)-2-phthalimido-1-nitrobenzeneHCID 18174472—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product5-(Tert-butyldimethylsilyloxy)-2-phthalimidoanilineHCID 1817449489%

Reaction Steps

A suspension of 5-(tert-butyldimethylsilyloxy)-2-phthalimido-1-nitrobenzene (5.00 g, 12.5 mmol) and 10% palladium-on-carbon (2.5 g) in ethyl acetate (60 mL) was stirred under 1 atm of hydrogen for 16 h. The mixture was filtered through a pad of diatomaceous earth and concentrated in vacuo to yield 4.1 g (89%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500851B2
Source datasetuspto-grants-2002_12
ORD IDord-78ce9a51316c436a9a4d1f380610374c
Source noteuspto-grants-2002_12