HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048543Generated: October 26, 2026
Sodium triacetoxyborohydride → HCID 178434682, compound
https://huagongshe.com/reaction/2048543
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | (2R,6S)-2,6-dimethyloxan-4-one | HCID 10441716 | — |
| Reactant | HCID 178434684 | HCID 178434684 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178434682 | HCID 178434682 | 22% |
Reaction Steps
To a solution of 3-methyl-1H-1,2,4-triazol-5-amine (1.6 g) in acetic acid (30 mL) was added (2R,6S)-2,6-dimethyltetrahydro-4H-pyran-4-one (2.5 g) at room temperature, and the mixture was stirred for 30 min. Sodium triacetoxyborohydride (5.2 g) was added, and the mixture was stirred at room temperature for 20 hr. Acetic acid was evaporated and ethyl acetate and water were added to the residue. The mixture was neutralized with sodium hydrogen carbonate, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The residue was dissolved in a small amount of ethyl acetate, and the mixture was crystallized from diisopropyl ether. The resulting solid was collected by filtration, washed with diisopropyl ether, and dried by heating under reduced pressure to give the title compound as a pale-yellow solid (0.75 g, 22%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592431B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-edd90544216b400fad74f5fd08a2166c |
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| Source note | uspto-grants-2013_11 |
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