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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359647Generated: November 2, 2026

Thiophenol → 5-Phenylsulfanyl-[1,3,4]thiadiazole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1359647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 5-chloro-1,3,4-thiadiazole-2-carboxylateHCID 12348753—
SolventAcetonitrileHCID 6342—
Product5-Phenylsulfanyl-[1,3,4]thiadiazole-2-carboxylic acid ethyl esterHCID 6997468174.4%

Reaction Steps

To a solution of 5-chloro-[1,3,4]thiadiazole-2-carboxylic acid ethyl ester (1.0 g, 5.2 mmol, 1 eq), and K2CO3 (1.44 g, 104 mmol, 2 eq) in CH3CN (50 mL), thiophenol (0.53 mL, 5.2 mmol, 1 eq) is added. The reaction is stirred overnight at room temperature. The reaction is filtered to remove the salts, and the filtrate is washed with CH3CN. The solvents are removed under reduced pressure, and the product is recrystallized from EtOH to give 5-phenylsulfanyl-[1,3,4]thiadiazole-2-carboxylic acid ethyl ester (1.03 g, 74%). MS (ESI) for C11H10N2O2S2 m/z 267.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599916B2
Source datasetuspto-grants-2003_07
ORD IDord-7eecb3045b2245dd89d6bbfc0023f821
Source noteuspto-grants-2003_07