HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1498113Generated: October 28, 2026
Hydrazine, dihydrochloride → HCID 178419301, compound
https://huagongshe.com/reaction/1498113
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine, dihydrochloride | HCID 17548 | — |
| Reactant | HCID 58204579 | HCID 58204579 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178419301 | HCID 178419301 | 90.2% |
Reaction Steps
To a suspension of 8-bromo-4-[1-dimethylamino-meth-(E)-ylidene]-3,4-dihydro-2H-benzo[b]-oxepin-5-one (5.32 g, 17.9 mmol) in isopropyl alcohol (50 mL) was added powdered hydrazine dihydrochloride (3.77 g, 35.9 mmol) at room temperature, then the mixture stirred for 2 h. The reaction mixture was diluted with water (20 mL) and then heated at 100° C. for 2 h before cooling to room temperature. The reaction mixture was concentrated in vacuo to remove the volatile solvent. The resulting suspension was filtered and the filtrate washed with water and dried under vacuum at 40° C. to yield 8-Bromo-4,5-dihydro-2H-6-oxa-1,2-diaza-benzo[e]azulene as a pale yellow solid (4.28 g, 90%). 1H NMR δ (ppm) (DMSO-d): 8.07 (1 H, d, J=8.52 Hz), 7.64 (1 H, s), 7.30-7.24 (1 H, m), 7.21 (1 H, d, J=2.07 Hz), 4.24 (2 H, dd, J=5.63, 4.50 Hz), 3.00 (2 H, t, J=5.09 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09198918B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-431f4f0993b746598f6de4a2f74cd7df |
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| Source note | uspto-grants-2015_12 |
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