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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412303Generated: November 3, 2026

Hydrochloric Acid → HCID 15583091, compound

https://huagongshe.com/reaction/2412303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhenyl isocyanateHCID 7672—
ReactantSodium hydrideHCID 24758—
ReactantHCID 20432881HCID 20432881—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15583091HCID 15583091—

Reaction Conditions

Temperature30 °C

Reaction Steps

13.2 g (0.077 mole) butyric acid-N-(1,2,3-thiadiazole-5-yl)-amide were dissolved in 150 ml absolute tetrahydrofuran and reacted with 3.36 g (0.077 mole) of a 55% dispersion of sodium hydride in oil, whereby during the addition the reaction solution through cooling is maintained at 30° C. After about 30 minutes of stirring at room temperature, the evolution of hydrogen is completed. 8.3 ml (0.077 mole) phenylisocyanate is added dropwise within about 5 minutes during which time the reaction temperature increases to 36° C. The reaction mixture is then stirred at room temperature for 1.5 hours whereby a thick crystaline slurry is formed. The reaction mixture is then introduced into a solution of 12.3 ml (0.154 mole) concentrated hydrochloric acid in 300 ml of water. Thereafter the reaction mixture is extracted with 250 ml acetic ester, the organic phase washed with water, dried over magnesium sulfate, filtered and concentrated in vacuum. There were thusly obtained colorless crystals which were digested with 50 ml diisopropylether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04491466
Source datasetuspto-grants-1985_01
ORD IDord-4d48a4527a3b4461b532883a37974ec6
Source noteuspto-grants-1985_01