HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(2-Bromoethoxy)-4-(tert-butoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | p-Tert-butoxyphenol | HCID 2773621 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-(2-Bromoethoxy)-4-(tert-butoxy)benzene | HCID 15018832 | 29.3% |
Reaction Steps
A solution of KOH (0.224 g, 4 mmol) in MeOH (3 mL) was added, over the course of 30 min, to a warmed (70° C.) mixture of 1,2-dibromoethane (3 g, 0.016 mol) and 4-(tert-butoxy)phenol (0.66 g, 0.004 mol). The mixture was stirred at 70° C. for 15 h before water and CHCl3 were added. The layers were separated, the organic layer washed with 10% aqueous NaOH and then dried (Na2SO4) and concentrated in vacuo to give 0.32 g (28%) of the sub-title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351821B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-088ac04fbafa4314b410de126c821bea |
| Source note | uspto-grants-2008_04 |