HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 19707365, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 57200436 | HCID 57200436 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19707365 | HCID 19707365 | 60% |
Reaction Steps
To the 6-fluoro 1-methyl-2-pyrrolidinyl-3,4-dihydronaphthalene afforded above in Step B in 1700 ml of ethyl acetate was added sodium acetate (10.2 g; 124.4 mmol), acetic acid (10.2 ml; 178.2 mmol) and 102 ml of water. The reaction mixture was stirred at room temperature for 4 hours. The layers were separated and the organic layer was washed with brine, 5% NaHCO3, and brine. The organic layer was dried over MgSO4 and was concentrated to afford 7.9 g of the subtitle compound as a dark orange-red oil (60% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05239075 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-2255c6c53b0441da8944679bbd6685d4 |
| Source note | uspto-grants-1993_08 |