HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 54366716, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Veratraldehyde | HCID 8419 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 10734538 | HCID 10734538 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54366716 | HCID 54366716 | 75.6% |
Reaction Steps
In 25 ml of methanol were suspended 2.0 g of methyl 2-hydroxy-4-methylsulfonylamino-5-phenoxyphenyl ketone and 1.03 g of 3,4-dimethoxybenzaldehyde. Thereto was added 5 ml of 50% aqueous sodium hydroxide. The mixture was stirred for 3 hours at room temperature. The reaction mixture was introduced into a mixture of 20 ml of ethyl acetate and 20 ml of water. The resulting mixture was adjusted to pH 2.0 with 4N hydrochloric acid. The resulting crystal was collected by filtration, washed with water and ethyl acetate in this order, and recrystallized from acetic acid to obtain 2.2 g (yield: 75.6%) of 2-(3,4-dimethoxyphenyl)vinyl 2-hydroxy-4-methylsulfonylamino-5-phenoxyphenyl ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04954518 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-c203daf487ee4cbbb0c09b6240df2af8 |
| Source note | uspto-grants-1990_09 |