HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Bromo-2-methoxyphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 53657601 | HCID 53657601 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Bromo-2-methoxyphenol | HCID 142228 | 98.3% |
Reaction Steps
A mixture of 4-bromo-2-methoxyphenyl benzoate (5 g), sodium hydroxide (3 g), water (5 mL) and ethanol (50 mL) is heated at reflux for 1.5 hours. It is then evaporated to low bulk and the resulting residue is treated with water (20 mL) and concentrated hydrochloric acid (10 mL), and extracted with dichloromethane (150 mL). The organic solution is extracted with saturated aqueous sodium bicarbonate solution (3×25 mL), dried over magnesium sulphate and evaporated, to give 5-bromo-2-methoxyphenol (3.25 g), in the form a colorless solid, m.p. 67°-68° C. [Elemental analysis: C,41.5; H,3.5; Br, 37.8%; calculated: C,41.6; H,3.5; Br, 39.5%].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05541219 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-e0f44e73107247df9ef78aa1f2629230 |
| Source note | uspto-grants-1996_07 |