HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 1-[3-(Ethyloxy)-4-nitrophenyl]-4-(1-methylethyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 1-(3-Ethoxy-4-nitrophenyl)piperazine | HCID 59452580 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 1-[3-(Ethyloxy)-4-nitrophenyl]-4-(1-methylethyl)piperazine | HCID 59452925 | 88% |
Reaction Steps
A mixture of 1-[3-(ethyloxy)-4-nitrophenyl]piperazine (Example 143, step A) (0.285 g, 1.13 mmol)) and acetone (0.13 g, 2.26 mmol) was stirred in DCE (5 mL) at rt under N2. To this mixture was added sodium triacetoxyborohydride (0.60 g, 2.8 mmol) and HOAc (0.136 g, 2.26 mmol). The reaction was stirred for approximately 24 h. The reaction was diluted with DCM and aqueous (saturated) NaHCO3. The aqueous layer was extracted with DCM (2×). The combined organic layers were dried over MgSO4, filtered, concentrated, and chromatographed on silica gel to give the title compound of step A (291 mg, 0.99 mmol, 88%) as a yellow solid. MS (ESI): 294 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08093239B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-27928e72e31643b3bacc1bac412b06e5 |
| Source note | uspto-grants-2012_01 |