HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294475Generated: October 27, 2026
4-Chloropyridine hydrochloride → 1-Amino-4-(4-pyridinyl)oxynaphthalene
https://huagongshe.com/reaction/1294475
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloropyridine hydrochloride | HCID 81852 | — |
| Reactant | 4-Amino-1-naphthol hydrochloride | HCID 2723858 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1-Amino-4-(4-pyridinyl)oxynaphthalene | HCID 23505862 | 16.5% |
Reaction Steps
To a stirred mixture of 4-amino-1-naphthol hydrochloride (2.5 g, 12.8 mmol) and 4-chloropyridine hydrochloride (3.84 g, 29.2 mmol) in NMP (20 ml) was added potassium tert-butoxide (6.0 g, 53.47 mmol) slowly. The mixture was heated at 120° C. for 6 h, cooled to room temperature and diluted with water and dichloromethane. The combined organic extracts were washed with HCl (2N), saturated aqueous NaHCO3 and brine and dried (Na2SO4). Removal of the volatiles in vacuo afforded the product (0.5 g, 16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07241758B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-9cf4d43925da4f3bb34d0e76054098e3 |
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| Source note | uspto-grants-2007_07 |
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