HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 21283634, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 13769240 | HCID 13769240 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21283634 | HCID 21283634 | — |
Reaction Steps
1-Phenyl-3-isoquinolinepropanoic acid (2 g) and concentrated sulphuric acid (2 cc) in absolute ethanol (20 cc) are stirred for 20 hours at room temperature (approximately 20° C.). The mixture is diluted with water (100 cc), alkalinised to pH 9 with concentrated ammonia solution and extracted with methylene chloride (3×50 cc). The organic phase is dried over magnesium sulphate, filtered and evaporated to dryness under reduced pressure. Ethyl 1-phenyl-3-isoquinolinepropionate (1.9 g) is obtained in the form of an oil, the proton NMR spectrum of which, in deuterated chloroform, has the following characteristics:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04788204 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-b46932b8b2de40589685054dda154190 |
| Source note | uspto-grants-1988_11 |