HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Dimethylamino)ethanol → (2-[4-(Tert-butyl)-2-nitrophenoxy]-ethyl)dimethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Dimethylamino)ethanol | HCID 7902 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Phenol, 4-(1,1-dimethylethyl)-2-nitro- | HCID 18661 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (2-[4-(Tert-butyl)-2-nitrophenoxy]-ethyl)dimethylamine | HCID 21959559 | — |
Reaction Steps
To a mixture of 2-nitro-4-tert-butylphenol (2 g) and N,N-dimethylethanolamine (1.3 g) and PPh3 (4 g) in THF (50 ml) was added DEAD (2.6 ml). The reaction was stirred at RT for 1 h, diluted with EtOAc (50 ml) and washed with 1 N HCl twice. The aqueous layer was basified with NaHCO3, extracted with EtOAc twice and washed with H2O and brine. The organic layer was dried over Na2SO4 and evaporated to give (2-[4-(tert-butyl)-2-nitrophenoxy]-ethyl)dimethylamine, was used in next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07687643B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-54221537a8fa4d239f331b3c74ee96ae |
| Source note | uspto-grants-2010_03 |