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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301874Generated: October 31, 2026

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

https://huagongshe.com/reaction/2301874

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 (ESD for C11H10N2O2S2 m/z 267.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500840B2
Source datasetuspto-grants-2002_12
ORD IDord-e0495d5931a941a6b396567f8016698b
Source noteuspto-grants-2002_12