Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506437Generated: November 3, 2026

Thionyl Chloride → HCID 68421991, compound

https://huagongshe.com/reaction/506437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68420889HCID 68420889—
SolventTolueneHCID 1140—
ProductHCID 68421991HCID 6842199158%

Reaction Steps

4-Cyclopropyl-1,2,3-thiadiazole-5-carboxamide (4 g; 24 mmols) was dissolved in toluene (15 ml), and thionyl chloride (5 ml) was added thereto, followed by refluxing for 10 hours under heating. After cooling to room temperature, ice was added thereto to stop the reaction, and sodium hydrogen carbonate was added thereto to neutralize, followed by extracting with ethyl acetate. After drying over anhydrous sodium sulfate, the solvent was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=20:1) to thereby obtain 2.1 g of 4-cyclopropyl-1,2,3-thiadiazole-5-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786040B2
Source datasetuspto-grants-2010_08
ORD IDord-652de6a6a4654b0b89869e573d324c15
Source noteuspto-grants-2010_08