HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246956Generated: October 30, 2026
Aluminium lithium hydride → 8-Fluoro-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine
https://huagongshe.com/reaction/1246956
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 21904832 | HCID 21904832 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-Fluoro-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine | HCID 21904830 | — |
Reaction Steps
THF (19.1 mL) was added to a flask containing 8-fluoro-3,4-dihydro-1H-1,4-benzodiazepine-2,5-dione (2.11 g, 10.9 mmol). Dropwise over 10 minutes was added lithium aluminum hydride in 1M THF (48.9 mL, 48.9 mmol). The reaction mixture was heated to reflux for 5.5 hours, and then let cool to room temperature overnight. After 18 hours, no starting material was seen. The reaction was quenched with water, 15% sodium hydroxide and another portion of water. After the white precipitate was filtered off, THF was removed from the filtrate. The contents of the flask were then transferred to a separatory funnel using ethyl acetate and water, and extracted with ethyl acetate (3×). The combined organic extracts were washed with brine (1×) and then dried with magnesium sulfate, filtered and concentrated to give a yellow oil. Further purification (15% ammonia 2M solution in ethanol/ethyl acetate) yielded the desired compound.
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-086b9d38f42e4be3a28fdee193c7d48f |
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| Source note | uspto-grants-2006_10 |
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