HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromo-2-hydroxy-6-methoxybenzoic acid → 1-Bromo-4-methoxy-2-(methoxymethoxy)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromo-2-hydroxy-6-methoxybenzoic acid | HCID 13493838 | — |
| Reactant | 2-Bromo-5-methoxyphenol | HCID 13493839 | — |
| Solvent | Quinoline | HCID 7047 | — |
| Product | 1-Bromo-4-methoxy-2-(methoxymethoxy)benzene | HCID 14827037 | — |
Reaction Steps
1-Bromo-2-hydroxy-4-methoxybenzene. 3-Bromo-2-hydroxy-6-methoxybenzoic acid [T. de Paulis et. al., J. Med. Chem., (1985), 28, 1263-1269] (5 g, 0.02 mol) was heated in quinoline (200 mL) at 160° C. for 1 h. On cooling, the product was partitioned between Et2O and 3M HCl. The organic extract was washed with water and brine then dried (MgSO4), filtered and evaporated to give the title compound which was recrystallized from 5% ethyl acetate/hexane (4 g, 97%); m.p. 40°-42° C. Anal. Calc. for C7H7BrO2 : C, 41.41; H, 3.48. Found C, 41.39; H, 3.37.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05716984 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-b229ba1c7cc745c7a538fe83f9726d27 |
| Source note | uspto-grants-1998_02 |