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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589727Generated: November 3, 2026

Water → HCID 135590743, compound

https://huagongshe.com/reaction/1589727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 19770592HCID 19770592—
SolventEthanolHCID 702—
SolventHexaneHCID 8058—
ProductHCID 135590743HCID 13559074392.8%

Reaction Conditions

Temperature70 °C

Reaction Steps

1.59 g (24.1 mM) of 85%-potassium hydroxide was dissolved in 50 ml of ethanol on an oil bath (bath temperature: about 70° C.). To the solution, 3.37 g (wet, 8.90 mM) of 2-decyl-5-(4-acetoxy-3-fluorophenyl)-1,3,4-thiadiazole was added, followed by stirring for 10 minutes at about 70° C. After the reaction, the reaction mixture was poured into iced water, followed by filtration under reduced pressure. The filtrate was condensed, followed by successive addition of about 100 ml of water, 2.3 ml of concentrated sulfuric acid and common salt and stirring at room temperature to precipitate a crystal. The crystal was dissolved in ethyl acetate and dried with anhydrous sodium sulfuric acid. The sodium sulfuric acid was recovered by filtration and the filtrate was condensed into a solid; n-hexane was added to the solid and stirred at room temperature, followed by filtration to obtain 2.78 g of 2-decyl-5-(3-fluoro-4-hydroxyphenyl)-1,3,4-thiadiazole (Yield: 92.8%, Yield through the steps iii) and iv): 82.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05200109
Source datasetuspto-grants-1993_04
ORD IDord-96b6fb6f72e24e36b70b43cd24d51583
Source noteuspto-grants-1993_04