HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (4-Dimethylamino-4-phenylcyclohexylidene)acetic acid hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (4-Dimethylamino-4-phenylcyclohexylidene)acetic acid methyl ester hydrochloride | HCID 67386135 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (4-Dimethylamino-4-phenylcyclohexylidene)acetic acid hydrochloride | HCID 67386703 | 98% |
Reaction Steps
1.7 M KOH (70.5 ml, 120 mmol) was added to a solution of (4-dimethylamino-4-phenylcyclohexylidene)acetic acid methyl ester hydrochloride (1.8 g, 5.8 mmol) in ethanol (200 ml) and the mixture was stirred at RT for 16 h. The reaction mixture was concentrated and the residue was taken up in water (40 ml). The aqueous phase was extracted by shaking with ether (2×40 ml), and 5.5 M hydrochloric acid (23.6 ml, 130 mmol) was added. After the aqueous phase had been concentrated, the residue was extracted with ethanol (2×40 ml), the potassium chloride which remained was separated off and the filtrate was concentrated. The hydrochloride of the acid was thereby obtained as a colourless solid in a yield of 98% (1.67 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08017630B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-c1b813893309407887b16d63fe4d1012 |
| Source note | uspto-grants-2011_09 |