HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746204Generated: October 30, 2026
Hydrochloric Acid → HCID 13289763, compound
https://huagongshe.com/reaction/746204
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13289762 | HCID 13289762 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13289763 | HCID 13289763 | 75.4% |
Reaction Steps
13.2 g (0.05 mol) of 1-cyclohexyl-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-pentan-3-one are dissolved in a mixture of 100 ml of methanol and 20 ml of water, a total of 2 g (0.05 mol) of sodium borohydride is added in several portions, and the mixture is stirred overnight. To work up the reaction mixture, it is brought to pH 5 with dilute hydrochloric acid, and the solvent is evaporated off in vacuo. The residue is taken up in water and extracted several times with methylene chloride. The combined organic extracts are washed with sodium bicarbonate solution and water, dried over sodium sulphate and evaporated down in vacuo. The residue is crystallized using petroleum ether. 10 g (75.2% of theory) of 1-cyclohexyl-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-pentan-3-ol are obtained in the form of colorless crystals of melting point 104° C. to 107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04603140 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-04aa2a6acad64f5ba0b0320f9a77b5f5 |
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| Source note | uspto-grants-1986_07 |
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