HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → 5-Phenylsulfanyl-[1,3,4]thiadiazole-2-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate | HCID 12348753 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Phenylsulfanyl-[1,3,4]thiadiazole-2-carboxylic acid ethyl ester | HCID 69974681 | 74.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06492385B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-5bb4b57b484f43a5920e7fb5b389f464 |
| Source note | uspto-grants-2002_12 |