HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657580Generated: October 31, 2026
Carbon Tetrachloride → 5-Chloro-2-methoxy-3-pyridinecarbonyl chloride
https://huagongshe.com/reaction/1657580
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Chloro-2-methoxynicotinic acid | HCID 9836973 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5-Chloro-2-methoxy-3-pyridinecarbonyl chloride | HCID 20156610 | — |
Reaction Steps
To a suspension of 3.76 g. (0.02 mole) of 5-chloro-2-methoxynicotinic acid in 100 ml. of carbon tetrachloride, there were added 100 ml. of thionyl chloride in one portion and the resulting mixture was then refluxed on a steam bath for a period of 90 minutes. Upon completion of this step, the clear solution so obtained was cooled and then concentrated in vacuo at room temperature to afford a residual oil. The excess thionyl chloride present was next removed in the same manner as described in Preparation A for the production of 2-methoxynicotinoyl chloride, except that only 100 ml. of benzene was employed this time (i.e., during each purification step). The yield of pure 5-chloro-2-methoxynicotinoyl chloride, obtained as the residual product, was quantitative in this particular instance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03961065 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-da49a25e91114e4d8907dd163c963add |
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| Source note | uspto-grants-1976_06 |
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