HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903019Generated: October 30, 2026
Oxalyl chloride → HCID 20571271, compound
https://huagongshe.com/reaction/903019
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 20571255 | HCID 20571255 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20571271 | HCID 20571271 | — |
Reaction Steps
Oxalyl chloride (0.762 gram; 0.006 mole) is added dropwise to a suspension of N-(2-chloro-3-pyridyl)trifluoromethanesulfonamide (2.61 grams; 0.01 mole) and powdered molecular sieves (5.0 grams; Molecular Sieve, Type 3A) in methylene chloride (75 mls) at 0° C. under a nitrogen atmosphere. The mixture is then heated to 60° C., held thereat for 3 hours, and then stirred at room temperature for 60 hours. The reaction mixture is filtered and the filtrate is evaporated to dryness. The resulting residue is extracted with diethyl ether, and the combined ethereal extracts are dried over anhydrous sodium sulfate. The dried ethereal extract is then separated and evaporated to obtain 2.33 grams (81% of theoretical) of crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04226738 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-28d3e0ec4e7c4c0baba797cef3c86684 |
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| Source note | uspto-grants-1980_10 |
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