HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477445Generated: October 26, 2026
Water → 10,11-Dihydrodibenzo(b,f)(1,4)oxazepine
https://huagongshe.com/reaction/477445
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | O-(o-Aminophenoxy)benzoic acid lactam | HCID 72374 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 10,11-Dihydrodibenzo(b,f)(1,4)oxazepine | HCID 648933 | 97.4% |
Reaction Steps
In a one liter three neck flask (argon atmosphere) was placed 50 ml of dry THF and 7.97 g (0.21 mole) of LAH. The suspension was stirred and a warm suspension of 29.57 g (0.14 mole) of 10,11-dihydro dibenz[b,f][1,4]oxazepine-11-one (Aldrich) in 500 ml of THF was added in a slow stream. The reaction mixture was stirred and heated to reflux for 3 hr. The reaction mixture was cooled and cautiously treated with 15 ml of water and 15 ml of saturated sodium sulfate solution. The mixture was stirred and heated to reflux for one hr. The solids were removed by filtration and washed with THF. The filtrate was concentrated to dryness to give 26.90 g of an oil that crystallized on standing. The nearly pure crystalline product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04888335 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-81cb25eca54644d9be8c65a825ca28b0 |
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| Source note | uspto-grants-1989_12 |
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