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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044273Generated: November 1, 2026

Hydrazine, dihydrochloride → HCID 178419301, compound

https://huagongshe.com/reaction/2044273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine, dihydrochlorideHCID 17548—
ReactantHCID 58204579HCID 58204579—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 178419301HCID 17841930190.2%

Reaction Conditions

Temperature100 °C

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 (1H, d, J=8.52 Hz), 7.64 (1H, s), 7.30-7.24 (1H, m), 7.21 (1H, d, J=2.07 Hz), 4.24 (2H, dd, J=5.63, 4.50 Hz), 3.00 (2H, t, J=5.09 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586574B2
Source datasetuspto-grants-2013_11
ORD IDord-0292c8cdfc6d45bd801b3b43becdfdf6
Source noteuspto-grants-2013_11