HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → 6-Benzylpyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | 2-(Phenylmethyl)pyridine | HCID 7581 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Product | 6-Benzylpyridin-2-amine | HCID 93902 | — |
Reaction Steps
Example 298 A) A sample of 2-benzylpyridine (Aldrich, 2.5 g, 0.015 mole), sodium amide (780 mg, 0.02 mole) and N, N-dimethylaniline (25 mL) were refluxed overnight. The contents were allowed to cool and were partitioned between ether and water. The ether layer was dried (MgSO4) and concentrated in vacuo leaving an oil. The oil was purified by chromatography. The purified material was dissolved in 1N HCl, lyophilized, and triturated with EtOAc to give 2-amino-6-benzylpyridine as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06011028 |
| Source dataset | uspto-grants-2000_01 |
| ORD ID | ord-1d26b230ebcc4fa8ac3b368b912322b7 |
| Source note | uspto-grants-2000_01 |