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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261305Generated: November 2, 2026

Hydrochloric Acid → HCID 57736332, compound

https://huagongshe.com/reaction/2261305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86631041HCID 86631041—
SolventEthanolHCID 702—
ProductHCID 57736332HCID 57736332—

Reaction Steps

Then, the resulting {[2-(2-propynyloxy)-1,3-thiazol-5-yl]methylidene}malononitrile was dissolved in 20 ml of ethanol, and a suspension of 0.09 g of sodium borohydride in 1 ml of ethanol was added dropwise. The mixture was stirred at room temperature for 1 hour. After 10 ml of 3% hydrochloric acid was added, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with aqueous saturated sodium chloride, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure to obtain 1.55 g of {[2-(2-propynyloxy)-1,3-thiazol-5-yl]methyl}.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846956B2
Source datasetuspto-grants-2010_12
ORD IDord-1c07b3e5999f4a41ac53501a33a31223
Source noteuspto-grants-2010_12