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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065789Generated: November 1, 2026

Sodium borohydride → HCID 54195003, compound

https://huagongshe.com/reaction/1065789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 54267703HCID 54267703—
SolventMethanolHCID 887—
ProductHCID 54195003HCID 5419500349.4%

Reaction Steps

85 g (0.27 mole) of 4,4-dimethyl-1-(naphth-2-yl)-2-(1,2,4-triazol-1-yl)-1-penten-3-one (Example 1) were taken up in 200 ml of methanol, and 6 g of sodium borohydride were added in portions, while stirring and cooling. When the reaction had ended, the reaction mixture was adjusted to pH 6 and concentrated. The residue was taken up in methylene chloride, washed with saturated sodium bicarbonate solution, dried over sodium sulphate, filtered and concentrated. The oily residue was made to crystallized by adding ether. 41 g (49% of theory) of 4,4-dimethyl-1-(naphth-2-yl)-2-(1,2,4-triazol-1-yl)-1-penten-3-ol of melting point 122°-124° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04331675
Source datasetuspto-grants-1982_05
ORD IDord-797603af6e9b4b34a9c6cb3d040ae6bd
Source noteuspto-grants-1982_05