HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975130Generated: November 2, 2026
Sodium borohydride → HCID 18920258, compound
https://huagongshe.com/reaction/1975130
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(3-(3-Methyl-2-butenyloxy)-1,2,5-thiadiazol-4-yl)-1-methylpyridinium iodide | HCID 19075389 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18920258 | HCID 18920258 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05284859 |
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| Source dataset | uspto-grants-1994_02 |
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| ORD ID | ord-ff463001b0e9491fa1c128e976728743 |
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| Source note | uspto-grants-1994_02 |
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