HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633602Generated: October 25, 2026
Potassium Carbonate → Ethyl 4-(3-(1-methylpiperidin-3-yl)phenylamino)-3-nitrobenzoate
https://huagongshe.com/reaction/1633602
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-chloro-3-nitrobenzoate | HCID 1268247 | — |
| Reactant | HCID 22741929 | HCID 22741929 | — |
| Product | Ethyl 4-(3-(1-methylpiperidin-3-yl)phenylamino)-3-nitrobenzoate | HCID 22741906 | 98% |
Reaction Steps
A mixture of 1c (5.7 g, 25 mmol), 2j (3.8 g, 20 mmol) and potassium carbonate (3.45 g, 25 mmol) was heated to 70° C. under a stream of nitrogen. The resulting melt was stirred at 70° C. overnight. The reaction mixture was partitioned between water and ethyl acetate and the organic phase was extracted with diluted hydrochloric acid (4M). The aqueous phase was rendered alkaline by addition of aqueous sodium hydroxide (4M) and extracted with ethyl acetate. The organic phase was dried over sodium sulfate and the solvent was removed under reduced pressure to leave ethyl 4-(3-(1-methylpiperidin-3-yl)phenylamino)-3-nitrobenzoate (7.5 g, 98%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06503925B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-d53fe524b96b48ebb269cb5f7d58a262 |
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| Source note | uspto-grants-2003_01 |
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