HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254415Generated: November 1, 2026
HCID 19744589, compound → HCID 19744627, compound
https://huagongshe.com/reaction/2254415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 19744589 | HCID 19744589 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 19744627 | HCID 19744627 | 69.2% |
Reaction Steps
430 mg of ethyl 3-(1,3,4-triazol-1-yl)benzoate [synthesized substantially in accordance with the method described in J. Med. Chem., 5, 383 (1962)] was dissolved in a mixture of 20 ml of tetrahydrofuran and 20 ml of dioxane, and 100 mg of lithium aluminium hydride was added. The mixture was stirred at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure, and the residue was distributed between ethyl acetate and water. The organic layer was separated and dried over anhydrous sodium sulfate. The desiccant was separated by filtration, and the solvent evaporated. The residue was purified by silica gel column chromatography [Wakogel C-200, 20 g; eluting solvent: chloroform/methanol=20/1] to give 240 mg (yield 69%) of 1(3-hydroxymethylphenyl)-1,3,4-triazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05234946 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-a29c444c0fac40a7a8ea1d18f4247b3f |
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| Source note | uspto-grants-1993_08 |
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