HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341505Generated: November 2, 2026
Hydrochloric Acid → HCID 59354899, compound
https://huagongshe.com/reaction/341505
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-Furanol, tetrahydro- | HCID 9960 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Chloronicotinic acid | HCID 79222 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 59354899 | HCID 59354899 | — |
Reaction Steps
To 6-chloro-nicotinic acid (415 mg, 2.59 mmol), was added 3-hydroxytetrahydrofuran (468 mg, 5.16 mmol), potassium hydroxide (579 mg, 10.3 mmol) and DMSO (5 mL). The mixture was heated at 120 C for 24 h. Further potassium hydroxide (579 mg) and 3-hydroxytetrahydrofuran (468 mg) was added and the mixture heated at 120 C for 24 h. The reaction was allowed to cool to room temperature, acidified to pH=1-2 with a 2M aq. solution of HCl (13 mL) and extracted into EtOAc (3×5 mL). The combined extracts were washed with water (5×20 mL), saturated brine (2×20 mL) and dried over anhydrous sodium sulfate. Evaporation of the solvent afforded the title compound as an orange solid which was dried under high vacuum to remove traces of solvent (209 mg, 39%). Method B HPLC-MS: MH+ requires m/z=210. Found: m/z=210, Rt=1.32 min (100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895733B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-f4385c1563e546e0a37d7d481efc84cb |
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| Source note | uspto-grants-2014_11 |
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