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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5533Generated: October 26, 2026

1-Chloro-4-nitrobenzene → 3,5-Bis-(4-nitrophenylthio)-1,2,4-thiadiazole

https://huagongshe.com/reaction/5533

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-nitrobenzeneHCID 7474—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178418624HCID 178418624—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3,5-Bis-(4-nitrophenylthio)-1,2,4-thiadiazoleHCID 1979614492%

Reaction Conditions

Temperature100 °C

Reaction Steps

3 g of NaOH were dissolved in 5 ml of water in a 250 ml three-necked flask, 3.8 g (25 mmol) of 3,5-dimer-capto-1,2,4-thiadiazole (preparation analogous to U.S. No. 3,899,502 or Z. Anorgan. Allgem. Chemie volume 486 (1982), pages 111-115) were added and the mixture was heated to 100° C. 79 g (50 mmol) of 1-chloro-4-nitrobenzene, dissolved in 75 ml of DMF, were metered into the clear solution. After the mixture had been boiled under reflux for 4 hours, it was evaporated and the residue was taken up in water, washed and filtered off. After recrystallization from an acetone-water mixture, 9 g (92% of theory) of 3,5-bis-(4-nitrophenylthio)-1,2,4-thiadiazole were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244999
Source datasetuspto-grants-1993_09
ORD IDord-fc2653c706e943b8b80ddf6fb2c55f7f
Source noteuspto-grants-1993_09