HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419546Generated: October 31, 2026
Sodium borohydride → 2-(Methyloxy)-4-(4-propyl-1-piperazinyl)aniline
https://huagongshe.com/reaction/419546
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-[3-(Methyloxy)-4-nitrophenyl]-4-propylpiperazine | HCID 59860266 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 2-(Methyloxy)-4-(4-propyl-1-piperazinyl)aniline | HCID 59860282 | 93.2% |
Reaction Steps
A mixture of 1-[3-(methyloxy)-4-nitrophenyl]-4-propylpiperazine (0.204 g, 0.73 mmol) and nickel(II) chloride hexahydrate (0.087 g, 0.37 mmol) was stirred in 2:1 MeOH/THF (7 mL) under N2 at rt. To this mixture was added NaBH4 (0.097 g, 2.6 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 (170 mg, 0.68 mmol, 93%) as a grey oil. 1H NMR (400 MHz, DMSO-d6): δ 6.50 (d, 1H, J=8.25), 6.47 (d, 1H, J=2.38 Hz), 6.26 (dd, 1H, J=2.47 and 8.34 Hz), 4.19 (br s, 2H), 3.72 (s, 3H), 2.90-2.94 (m, 4H), 2.43-2.47 (m, 4H), 2.25 (t, 2H, J=7.42 Hz), 1.44 (q, 2H, J=7.39 Hz), 0.86 (t, 3H, J=7.33 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093239B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-e2d9e258f36c416592c274de253c04f0 |
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| Source note | uspto-grants-2012_01 |
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