HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tin chloride monohydrate → 4-(3-Ethoxyphenoxy)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tin chloride monohydrate | HCID 45051637 | — |
| Reactant | 1-Ethoxy-3-(4-nitrophenoxy)benzene | HCID 67234996 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(3-Ethoxyphenoxy)aniline | HCID 26189742 | 82% |
Reaction Steps
A solution of 1-(ethyloxy)-3-[(4-nitrophenyl)oxy]benzene (Intermediate 3, 4 g) and tin chloride monohydrate (28.8 g, 139 mmol) in ethyl acetate (200 mL) was heated at reflux overnight (15 hours). The reaction mixture was cooled down. It was then diluted with ethyl acetate (50 mL), washed with saturated NaHCO3 (100 mL), brine (100 mL) and dried over sodium sulphate. After evaporation of the volatiles, the residue was purified by an SCX (wash of the column with methanol, adsorption of the compound, wash with methanol (3CV), desorption with 2N methanolic ammonia (3CV)). Evaporation afforded the title compound (2.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722695B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-0d80d0db0ff443f4aa582783b860131b |
| Source note | uspto-grants-2014_05 |