HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (2-(Ethyloxy)-4-[4-(1-methylethyl)-1-piperazinyl]phenyl}amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-[3-(Ethyloxy)-4-nitrophenyl]-4-(1-methylethyl)piperazine | HCID 59452925 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | (2-(Ethyloxy)-4-[4-(1-methylethyl)-1-piperazinyl]phenyl}amine | HCID 59452785 | 93% |
Reaction Steps
A mixture of 1-[3-(ethyloxy)-4-nitrophenyl]-4-(1-methylethyl)piperazine (0.285 g, 0.97 mmol) and nickel(II) chloride hexahydrate (0.116 g, 0.48 mmol) was stirred in 2:1 MeOH/THF (10 mL) under N2 at rt. To this mixture was added NaBH4 (0.129 g, 3.4 mmol) in 2 equal portions over 5 min. The reaction was stirred at rt for about 45 min, then concentrated under vacuum. The residue was dissolved in DCM and poured through Celite, washing with DCM and EtOAc. The filtrate was concentrated and chromatographed on silica gel to give the title compound of step B (238 mg, 0.90 mmol, 93%) as a grey oil. MS (ESI): 264 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08093239B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-57603de864ea42a09709ce1157cdd1bd |
| Source note | uspto-grants-2012_01 |