HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557166Generated: October 28, 2026
Water → 2,3,4,5-tetrahydro-1H-1-benzazepine
https://huagongshe.com/reaction/557166
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1,3,4,5-Tetrahydro-2H-1-benzazepin-2-one | HCID 248580 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,3,4,5-tetrahydro-1H-1-benzazepine | HCID 576503 | 85% |
Reaction Steps
Add 80 mL of lithium aluminum hydride (1 M solution in tetrahydrofuran) to a solution of 1,3,4,5-tetrahydrobenzo-[b]azepin-2-one (12.9 g, 80.0 mmol) in 720 mL of tetrahydro-furan. Stir the reaction mixture at reflux for 3 hours and cool to 0° C. Quench the reaction by the sequential addition of 3 mL of water, 3 mL of 15% sodium hydroxide, and 9 mL of water. Filter the resulting suspension through Celite and rinse the filter cake with ethyl acetate. Concentrate the filtrate under reduced pressure to provide the desired compound as an orange solid (10.0 g, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08058425B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-1fdb39a98b5d4f6cba741c13dc313904 |
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| Source note | uspto-grants-2011_11 |
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