HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → (1-Bromonaphthalen-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Bromo-2-naphthalenemethanol acetate | HCID 13113199 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | (1-Bromonaphthalen-2-yl)methanol | HCID 13113200 | 96.3% |
Reaction Steps
Potassium hydroxide (25.3 g, 0.45 mol) was added to a solution of 1-bromo-2-naphthalenemethanol acetate (105 g, 0.38 mol) in methanol (300 mL) at room temperature. The resulting yellow solution was stirred at room temperature for 3 hours, then diluted with water and a precipitate was formed. The mixture was extracted with ether (2×300 mL), and the combined organic layers were washed with water (250 mL), brine, dried over anhydrous magnesium sulfate and concentrated in vacuo. The pure product was obtained as a light yellow solid (86.8 g, 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04897405 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-4f26c98a44f848499412e17566def333 |
| Source note | uspto-grants-1990_01 |