HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532564Generated: October 26, 2026
Sodium Hydroxide → 5-Chloro-3-fluoropyridine-2-carbonyl chloride
https://huagongshe.com/reaction/1532564
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Chloro-3-fluoropyridine-2-carboxylic acid | HCID 11769070 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 5-Chloro-3-fluoropyridine-2-carbonyl chloride | HCID 22013557 | — |
Reaction Steps
71.38 g of 3-fluoro-5-chloro-2-pyridinecarboxylic acid is initially introduced into a round-bottomed flask and heated up to 90° C. 59 ml of thionyl chloride are added dropwise from a dropping funnel in the course of 30 minutes, and the gas formed is passed into sodium hydroxide solution. The mixture is subsequently stirred at 100° C. for a further 5 hours. The thionyl chloride is then distilled off under normal pressure. After addition of 50 ml of dry toluene, 20 ml thereof are distilled off. The solution thus obtained is poured onto 200 ml of n-hexane and the mixture is stirred overnight. After cooling in an ice-bath, the mixture is filtered and the material on the filter is washed twice with n-hexane. 68.7 9 of the desired compound are obtained as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06204221B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-12a1ee2b1c304a3e8e25187ab19d91cc |
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| Source note | uspto-grants-2001_03 |
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