HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624054Generated: November 2, 2026
Hydrazinium chloride → HCID 178426391, compound
https://huagongshe.com/reaction/1624054
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazinium chloride | HCID 115031 | — |
| Reactant | HCID 71114823 | HCID 71114823 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178426391 | HCID 178426391 | — |
Reaction Steps
Hydrazine hydrochloride (0.14 g, 2 mmol) is added to 4-[(2Z)-2-(dimethylaminomethylene)-4,4-dimethyl-3-oxo-cyclohexyl]-3-methyl-benzonitrile (0.2 g, 0.67 mmol) in ethanol (30 mL), then acetic acid (two drops) is added to the mixture. After the addition is complete, the reaction mixture is stirred at 80° C. for 3 h. The mixture is cooled to room temperature and concentrated in vacuo. The residue is diluted with ethyl acetate (50 mL) and saturated sodium bicarbonate solution (50 mL). The organic phase is separated and the aqueous phase extracted with ethyl acetate (3×50 mL). The combined organic phase is washed with brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The residue is purified by silica gel column chromatography (eluted with pet ether:EtOAc=2:1 to 1:1) to give the title compound. The product is added to HCl/ethyl acetate and concentrated in vacuo to give the HCl salt of the title compound (0.12 g, 67%). ES/MS 266 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08778984B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-67a5d19738b74ac090cffd9b7865c43f |
|---|
| Source note | uspto-grants-2014_07 |
|---|