HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-Bromo-2-methoxyphenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18971766 | HCID 18971766 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Bromo-2-methoxyphenol | HCID 262234 | 195.4% |
Reaction Steps
A suspension of (20.7 g, 47.9 mmol, 1.0 eq) bis(2-methoxy-5-bromophenyl)carbonate in 250 ml methanol and 60 ml (120 mmol, 2.5 eq) of 2N NaOH was refluxed for 2 hours. The reaction mixture was cooled to room temperature, concentrated to a volume of ca 100 ml, and poured into 1 L of H2O. The pH was adjusted to 2 using 1N HCl. The acidic mixture was transferred to a separatory funnel, and extracted three times with ether. The ether extracts were combined and washed once with H2O, once with brine, and then dried over anhydrous sodium sulfate. Filtration, concentration and drying afforded 19.0 g of a white solid, which was recrystallized from petroleum ether to yield 17.63 g, 91% yield, of white prisms.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05563143 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-85885bf756c6419799ee2a01ba48613d |
| Source note | uspto-grants-1996_10 |