HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385523Generated: October 30, 2026
Water → (5,6,7,8-Tetrahydroquinoxalin-2-yl)methanol
https://huagongshe.com/reaction/385523
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 5,6,7,8-tetrahydroquinoxaline-2-carboxylate | HCID 57815216 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5,6,7,8-Tetrahydroquinoxalin-2-yl)methanol | HCID 57815285 | 78.5% |
Reaction Steps
To a solution of 0.16 g of ethyl 5,6,7,8-tetrahydroquinoxaline-2-carboxylate in 1.5 mL of tetrahydrofuran, 29 mg of lithium aluminum hydride was added under cooling with ice, the mixture was stirred for 45 minutes, 29 mg of lithium aluminum hydride was further added thereto, and the mixture was stirred for 30 minutes. Thereto were added ethyl acetate and water, the insoluble substance was filtered off, sodium chloride was added to a filtrate, the organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed with a saturated aqueous sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain 0.10 g of (5,6,7,8-tetrahydroquinoxalin-2-yl)methanol as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367831B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-9ee83d6333d9471bbe420832069d8bbc |
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| Source note | uspto-grants-2013_02 |
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