HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462649Generated: October 25, 2026
3-Hydroxypyridine → 3-Pyridyl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate
https://huagongshe.com/reaction/462649
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Hydroxypyridine | HCID 7971 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(2-Chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoyl chloride | HCID 3017765 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Pyridyl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate | HCID 13475656 | 70.7% |
Reaction Steps
To a stirred solution of 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoyl chloride (3.79 g, 0.01 mole) and triethyl amine (1.01 g, 0.01 mole) in toluene (50 ml) was added 3-hydroxypyridine (0.95 g, 0.01 mole). The temperature exothermed to 33° C. and there was an immediate precipitate. The reaction was then refluxed for 24 hours, cooled to room temperature and the triethylamine hydrochloride precipitate collected by filtration. The toluene solution was washed with dilute sodium hydroxide solution and then with saturated sodium chloride solution. After drying and evaporation of the solvent there was obtained 3.1 g of brown oil which solidified. This was triturated with hexane and the solid filtered and dried to give a tan product, m.p. 65°-68° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04517010 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-db7961b217924eacadb71753c875ceb0 |
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| Source note | uspto-grants-1985_05 |
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