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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903019Generated: October 30, 2026

Oxalyl chloride → HCID 20571271, compound

https://huagongshe.com/reaction/903019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 20571255HCID 20571255—
SolventDichloromethaneHCID 6344—
ProductHCID 20571271HCID 20571271—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04226738
Source datasetuspto-grants-1980_10
ORD IDord-28d3e0ec4e7c4c0baba797cef3c86684
Source noteuspto-grants-1980_10