HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(4-Chloro-phenoxymethyl)-benzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | 4-(4-Chlorophenoxymethyl)-benzylazide | HCID 23132437 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(4-Chloro-phenoxymethyl)-benzylamine | HCID 23132444 | — |
Reaction Steps
4-(4-Chloro-phenoxymethyl)-benzylazide (3.2 g, 11.7 mmol) was dissolved in MeOH (50 mL). NEt3 (11.35 mL, 81.9 mmol) and SnCl2×2H2O (5.28 g, 23.4 mmol) were added and the exothermic reaction was stirred under reflux. When boiling ceased the mixture was heated to reflux for additional 45 min. After cooling to r.t. the mixture was filtered and the filtrate was evaporated to dryness. The residue was dissolved in CH2Cl2 (300 mL) and this solution was washed with sat. aq. NaHCO3-solution (1×100 mL), dried over Na2SO4, filtered and evaporated to dryness to give the title compound, pure enough for further reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450348B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-5dc0a59858f2425ea9ecd12ec1d888fd |
| Source note | uspto-grants-2013_05 |