HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-((2-Nitrobenzyl)amino)propan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Amino-1-propanol | HCID 9086 | — |
| Reactant | 2-Nitrobenzyl chloride | HCID 11921 | — |
| Reactant | Hydrate;hydrochloride | HCID 21885828 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-((2-Nitrobenzyl)amino)propan-1-ol | HCID 28715654 | 33.2% |
Reaction Steps
3-Aminopropanol (3.94 g, 52.5 mmol) and triethylamine (1.77 g, 17.5 mmol) were dissolved in tetrahydrofuran (30 ml) and added with 2-nitrobenzyl chloride (3.00 g, 17.5 mmol) at room temperature. After heated to reflux for seven hours, the reaction mixture was allowed to cool and poured into 1N hydrochloric acid water and extracted with ether. The aqueous layer was adjusted to pH 9 with a saturated sodium hydrogen carbonate aqueous solution and then extracted with ethyl acetate. The organic layer was washed with a saturated brine and then dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to obtain 3-(2-nitrobenzylamino)propanol (1.22 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08048825B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-9355c83804f84ceca67ec9a7ac6706c6 |
| Source note | uspto-grants-2011_11 |