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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981457Generated: November 3, 2026

Sodium borohydride → Triapenthenol

https://huagongshe.com/reaction/1981457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(E)-1-cyclohexyl-2-(1,2,4-triazol-1-yl)-4,4-dimethyl-1-penten-3-oneHCID 12763477—
SolventMethanolHCID 887—
ProductTriapenthenolHCID 643784255.1%

Reaction Steps

26 g (0.1 mol) of (E)-1-cyclohexyl-4,4-dimethy-2-(1,2,4-triazol-1-yl)-pent-1-en-3-one are taken up in 200 ml of methanol, and 4.5 g of sodium borohydride are added in portions, while stirring and cooling. When the reaction has ended, the reaction mixture is brought to pH 6 and concentrated. The residue is taken up 200 ml of methylene chloride, the mixture is washed with saturated sodium bicarbonate solution, dried over sodium sulphate and filtered and the filtrate is concentrated. The residue is recrystallised from petroleum ether. 14.5 g (55% of theory) of racemic (E)-1-cyclohexyl-4,4-dimethyl-3-hydroxy-2-(1,2,4-triazol-1-yl)-pent-1-ene of melting point 131° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04592772
Source datasetuspto-grants-1986_06
ORD IDord-63aca424864648d3b63fb5255bd29527
Source noteuspto-grants-1986_06