HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 14032101, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Phenylhydrazine hydrochloride | HCID 60962 | — |
| Reactant | 5-Methoxy-4,6-dimethyl-2,3-dihydro-1H-inden-1-one | HCID 14032100 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14032101 | HCID 14032101 | — |
Reaction Steps
A mixture of 5-methoxy-4,6-dimethyl-1-indanone (3.0 g, 16 mmol) and phenylhydrazine hydrochloride (2.3 g, 16 mmol) was heated to reflux in ethanol (20 cm3) containing concentrated hydrochloric acid (2 cm3). The reaction mixture was heated at reflux for 6 hours, and cooled to room temperature. Water was added, and the resulting precipitate filtered off. This product was dried in a vacuum oven, and purified by column chromatography to yield the title compound as a colourless solid. Yield: 2.8 g, (67%). M.p. 177° C. from ethyl acetate petrol (60°-80° C.). 1H NMR (CDCl3)δ: 2.36 (6H, s,), 3.56 (2H, s,), 3.76 (3H, s,), 7.1-7.6 (5H, m,), 8.2 (1H,br,).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05185360 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-5c9ef2aee0604244bd283feed5706596 |
| Source note | uspto-grants-1993_02 |