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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807251Generated: November 1, 2026

Ammonium Chloride → 1-(4-Aminophenyl)-2-(tert-butyldimethylsilyloxy)ethanone

https://huagongshe.com/reaction/1807251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(Tert-butyldimethylsilyloxy)-1-(4-nitrophenyl)ethanoneHCID 19964186—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
Product1-(4-Aminophenyl)-2-(tert-butyldimethylsilyloxy)ethanoneHCID 5924955982.4%

Reaction Steps

Step B To a solution of 2-(tert-butyldimethylsilyloxy)-1-(4-nitrophenyl)ethanone (0.54 g, 1.83 mmol) in methanol (60 mL) was added an aqueous solution (15 mL) of ammonium chloride (0.98 g, 18.3 mmol), followed by the addition of Zinc (1.2 g, 18.3 mmol). The reaction mixture was stirred at room temperature for 1 h. The mixture was filtered through a short pad of celite. The filtrate was concentrated to a small volume, then when partitioned between ethyl acetate and water. The organic layer was separated, the aqueous layer was extracted with ethyl acetate. The organic layers were combined, washed with water, brine, dried over MgSO4, and concentrated to give 1-(4-amino-phenyl)-2-(tert-butyl-dimethyl-silanyloxy)-ethanone as a white foam (0.4 g, 82%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354444B2
Source datasetuspto-grants-2013_01
ORD IDord-9a8dc33c17f045efa960916bd0998f01
Source noteuspto-grants-2013_01