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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577619Generated: November 4, 2026

Oxalyl chloride → HCID 20571271, compound

https://huagongshe.com/reaction/1577619

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 Type 3A molecular sieves (5.0 grams) in dichloromethane (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 numberUS04288592
Source datasetuspto-grants-1981_09
ORD IDord-1ac0154a45b94948ae720e94f5ed487d
Source noteuspto-grants-1981_09