HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888095Generated: October 30, 2026
Sodium Hydroxide → 5,5-dimethyl-2,3,4,5-tetrahydro-1H-1-benzazepine
https://huagongshe.com/reaction/888095
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 5,5-Dimethyl-1,3,4,5-tetrahydro-benzo[b]azepin-2-one | HCID 57006474 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5,5-dimethyl-2,3,4,5-tetrahydro-1H-1-benzazepine | HCID 57470255 | — |
Reaction Steps
5,5-Dimethyl-1,3,4,5-tetrahydro-benzo[b]azepin-2-one (1.5 g, 8.0 mmol) was dissolved into THF (20 ml) and cooled down to 0° C. LAH (0.5 g 60% in oil, 13 mmol) was added in portions. The reaction was heated to reflux for 2 h. TLC showed a new spot alongside staring lactam. Another 360 mg of LAH was added and the mixture was heated for 2 h. H2O was added until sizzling stopped followed by 2N NaOH. Stirred for 15 min at RT. Na2SO4 (3.8 g) was added and the mixture was stirred for 15 min followed by filtration over Celite®. Diluted with EtOAc and washed with H2O, dried (MgSO4), filtered and concentrated to give 5,5-Dimethyl-2,3,4,5-tetrahydro-1H-benzo[b]azepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247556B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-9d0d82ddc0e04ca0a25d7e7b44c8bde8 |
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| Source note | uspto-grants-2012_08 |
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