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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975130Generated: November 2, 2026

Sodium borohydride → HCID 18920258, compound

https://huagongshe.com/reaction/1975130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(3-(3-Methyl-2-butenyloxy)-1,2,5-thiadiazol-4-yl)-1-methylpyridinium iodideHCID 19075389—
SolventEthanolHCID 702—
ProductHCID 18920258HCID 18920258—

Reaction Conditions

Temperature-10 °C

Reaction Steps

Sodium borohydride (220 mg, 6 mmol) was added to a solution of 3-(4-(3-methyl-2-butenyloxy)-1,2,5-thiadiazol-3-yl)-1-methylpyridinium iodide (0.92 g, 2.3 mmol) in ethanol (99.9%, 15 ml) and the reaction mixture was stirred at -10° C. for 0.5 h. After evaporation the residue was dissolved solved in water and extracted with ethyl acetate. The dried organic phases were evaporated and the residue purified by column chromatography (Si02, eluent: ethyl acetate/methanol (4:1)). The title compound was crystallized as the oxalate salt from acetone to yield 380 mg. (M.p. 150°-151° C.; M+ : 265; Compound 27).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05284859
Source datasetuspto-grants-1994_02
ORD IDord-ff463001b0e9491fa1c128e976728743
Source noteuspto-grants-1994_02