HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Iodophenol → HCID 18008068, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Iodophenol | HCID 12272 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Bromomethylnaphthalene | HCID 70320 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18008068 | HCID 18008068 | — |
Reaction Steps
To a solution of 3-iodophenol (4.0 g, 18 mmol) in ethanol (40 mL) is added potassium hydroxide (1.0 g, 18 mmol) and 2-(bromomethyl) naphthalene (4.0 g, 18 mmol) and this mixture is refluxed overnight. The hot reaction is filtered and the filtrate is chilled in ice. The ensuing precipitate is collected by filtration to give the title compound. 1H NMR (300 MHz, CDCl3) δ 7.84-7.89 (m, 4H), 7.48-7.53 (m, 3H), 7.40 (d, 1H), 7.29-7.32 (m, 1H), 6.95-7.04 (m, 2H), 5.20 (s, 2H); MS (EI) 360 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE040558E1 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-3cc22ff38b5e4e379872fb0bb833343f |
| Source note | uspto-grants-2008_10 |