HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715340Generated: October 30, 2026
Hydrochloric Acid → 6-(2,2,2-Trifluoroethoxy)pyridine-3-carboxylic acid
https://huagongshe.com/reaction/715340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Chloronicotinic acid | HCID 79222 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 6-(2,2,2-Trifluoroethoxy)pyridine-3-carboxylic acid | HCID 2781028 | 78% |
Reaction Steps
A mixture of 6-chloronicotinic acid (7.0 g, 44.4 mmol), 2,2,2-trifluoroethanol (6.40 mL, 89.0 mmol) and sodium hydride (5.33 g, 133.0 mmol, 60% in oil) in DMA (400 mL) is stirred at 90° C. for 21 hours. After cooling to rt, the reaction mixture is poured slowly into 2M hydrochloric acid (300 mL) and extracted with n-hexane/EtOAc (1:10, 500 mL). The organic layer is washed with 2 M hydrochloric acid (300 mL×2) and dried over sodium sulfate. The organic solvent is concentrated under reduced pressure to give 7.64 g (78% yield) of the title compound as colorless oil. This material is used for the next reaction (Step-2) without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187475B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-b3a48b270a404af3b681f757bc133774 |
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| Source note | uspto-grants-2015_11 |
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