HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 5-Fluoro-3-piperazino benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(5-Fluorobenzofuran-3-yl)-piperazine-1-carboxylic acid ethyl ester | HCID 59204839 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Fluoro-3-piperazino benzofuran | HCID 21471855 | 35.4% |
Reaction Steps
4-(5-fluorobenzofuran-3-yl)-piperazine-1-carboxylic acid ethyl ester (Step 1, 3 g) was dissolved in 95% ethanol and 3N aqueous sodium hydroxide (25 mL) was added. The reaction mixture was stirred at reflux for 24 hours. The mixture was then cooled to room temperature, concentrated on a rotary evaporator to remove the ethanol and extracted with chloroform. The combined organic layers were washed with brine, dried over anhydrous MgSO4, filtered and concentrated on a rotary evaporator. The desired product (0.8 g) was obtained as a brown oil and was used without further purification; MS (ES) m/z (relative intensity): 221 (M+H)+ (100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07671056B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-ba9a9fff95924b1099635ac2aea0ca82 |
| Source note | uspto-grants-2010_03 |