HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246959Generated: October 30, 2026
Aluminium lithium hydride → HCID 21904833, compound
https://huagongshe.com/reaction/1246959
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 21904838 | HCID 21904838 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21904833 | HCID 21904833 | — |
Reaction Steps
To a solution of 8-fluoro-7-methoxy-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione (5.1 g, 227 mmol) dissolved in THF (39.8 mL) was added lithium aluminum hydride (1M solution in THF, 102.4 mL, 102.4 mmol) dropwise. The reaction mixture was heated to reflux. After 26 hours, an additional equivalent of lithium aluminum hydride in THF (22.7 mmol) was added. At 30 hours, the reaction was quenched with water, 15% NaOH and an additional portion of water. The precipitate was filtered and washed with ethyl acetate. THF was removed from the filtrate, and then ethyl acetate and water were added to the flask. All the contents in the flask were transferred to the separatory funnel and extracted with ethyl acetate (3×). The combined organic layers were then washed with brine (1×), dried with magnesium sulfate, filtered and concentrated to give a brown oil. Further purification (15% ammonia in 2M solution of ethanol/ethyl acetate) yielded the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129237B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-8c66ea6886f54953875b921862ab373e |
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| Source note | uspto-grants-2006_10 |
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