HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → HCID 11992622, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | 3,5-Dimethoxyaniline | HCID 66301 | — |
| Reactant | 2-Bromo-1-(3,5-dimethoxyphenyl)ethanone | HCID 2756932 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 11992622 | HCID 11992622 | — |
Reaction Steps
0.32 g (2.1 mmoles) of 3,5-dimethoxyaniline, 0.26 g (1.0 mmol) of 2-bromo-1-(3,5-dimethoxyphenyl)ethanone and 0.42 ml (3.3 mmol) of N,N-dimethylaniline were placed in a vial. The vial was placed inside a monomode microwave reactor and was radiated at a power of 100 W, at a temperature of 150° C. for 10 minutes. After cooling the reaction vial, the mixture was dissolved in AcOEt, was washed with an aqueous HCl 2N solution, was dried on anhydrous Na2SO4 and was evaporated at low pressure. The crude portion was purified by means of pressure column chromatography (Eluent: AcOEt/hexanes) obtaining 4,6-dimethoxy-2-(3,5-dimethoxyphenyl)-1H-indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08097656B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-9bd8df5a8036493ab4bbe05e081921d1 |
| Source note | uspto-grants-2012_01 |