HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484222Generated: November 2, 2026
N,N-dimethyl-p-methoxybenzamide → 4-Methoxy-N,N-dimethylbenzylamine
https://huagongshe.com/reaction/1484222
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-dimethyl-p-methoxybenzamide | HCID 81713 | — |
| Reactant | o-Phenylenebis(dimethylsilane) | HCID 2733841 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Methoxy-N,N-dimethylbenzylamine | HCID 247495 | 96% |
Reaction Steps
A 20-mL eggplant flask equipped with a three-way cock and a magnetic stirrer was heat dried while pumping to a vacuum of 5 Pa before its interior was purged with argon atmosphere. Into the flask, iron complex A (1.0 mg, 0.002 mmol) was admitted as catalyst and dissolved in toluene (0.5 mL). To the solution, 1,2-bis(dimethylsilyl)benzene (475 μL) was added through a syringe, and N,N-dimethyl-4-methoxybenzamide (179 mg, 1.0 mmol) was added. The solution was stirred at 100° C. for 30 minutes. Toluene was distilled off in vacuum. The crude product was purified by silica gel-packed column chromatography using hexane/ethyl acetate (10/1) as developing solvent, obtaining N,N-dimethyl-4-methoxybenzylamine (159 mg, 0.96 mmol, 96%). The results are shown as Entry 1 in Table 5. The resulting amine was identified for geometry by 1H and 13C-NMR spectroscopy and IR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09421532B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-7d5935e94c3b450b84a82e3e6909a671 |
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| Source note | uspto-grants-2016_08 |
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