HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → [3-(4-bromophenoxy)propyl]dimethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | N,N-Dimethylaminoethyl chloride hydrochloride | HCID 11636816 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | [3-(4-bromophenoxy)propyl]dimethylamine | HCID 2183674 | — |
Reaction Steps
4-bromophenol (5.0 g, 28.9 mmol) and 2-dimethylaminoethyl chloride hydrochloride (4.6 g, 31.8 mmol) were combined in a mixture of toluene (100 mL) and 1 M NaOH (50 mL) and heated at reflux for 16 h. The layers were separated and the organic phase was washed with 1 M NaOH, dried (MgSO4) and concentrated to yield 4.2 g of the title compound as a yellow oil which was used without further purification. 1H NMR (400 MHz, CDCl3): δ 2.34 (6H, s), 2.72 (2H, t), 4. 01 (2H, t), 6.73 (2H, m), 7.33 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06693137B1 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-b5d840c0cc7d44b88e06198df65a1fca |
| Source note | uspto-grants-2004_02 |