HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 9947145, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2R,3R)-2,3-Dihydroxybutanedioic acid--3-{5-[(2R)-2-aminopropyl]-7-cyano-2,3-dihydro-1H-indol-1-yl}propyl benzoate (1/1) | HCID 45108224 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 9947145 | HCID 9947145 | 105.7% |
Reaction Steps
To a solution of potassium carbonate (32.3 g) in distilled water(120 ml) was added ethyl acetate (120 ml), and (R)-3-[5-(2-aminopropyl)-7-cyano-2,3-dihydro-1H-indol-1-yl]propyl benzoate L-tartrate (12.0 g) was added portionwise to the mixture with stirring. After reaction for 1 hour, the reaction mixture was extracted with ethyl acetate, and the ethyl acetate layer was washed with 10% aqueous potassium carbonate solution and brine subsequently, and dried over anhydrous sodium sulfate. The solvent was removed in vacuo to give (R)-3-[5-(2-aminopropyl)-7-cyano-2,3-dihydro-1H-indol-1-yl]propyl benzoate (8.98 g) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06310086B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-88d2bfca419a4061a60d592948c85c44 |
| Source note | uspto-grants-2001_10 |