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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-(Tert-butyldimethylsilyloxy)-1-(4-nitrophenyl)ethanone | HCID 19964186 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(4-Aminophenyl)-2-(tert-butyldimethylsilyloxy)ethanone | HCID 59249559 | 82.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354444B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-9a8dc33c17f045efa960916bd0998f01 |
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| Source note | uspto-grants-2013_01 |
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