HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851631Generated: November 2, 2026
4-Bromophenol → 2-(4-Bromophenoxy)-5-methoxybenzoic acid
https://huagongshe.com/reaction/1851631
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-5-methoxybenzoic acid | HCID 89906 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(4-Bromophenoxy)-5-methoxybenzoic acid | HCID 57475632 | — |
Reaction Steps
A RBF equipped with a reflux condenser was charged with 2-bromo-5-methoxy benzoic acid (430 g, 1.8614 mol), 4-bromo phenol (322 g, 1.8614 mol, 1 eq), potassium carbonate (514.5 g, 3.7 228 mol, 2.0 eq) and CuOTf-toluene complex (24.08 g, 0.04653 mol, 0.025 eq). Ethyl acetate (9.0 ml 0.09679 mol, 0.052) and toluene (1.3 L) was carefully added portion wise. After stirring at RT for 10 min, the mixture was heated to 50° C. and stirred for 30 min. The mixture was then heated to 110° C. for 20 hrs. The reaction was monitored by TLC. After 20 hrs, TLC showed total consumption of starting materials. The reaction mixture was cooled to RT, diluted with water and acidified by 2N HCl. The reaction mixture was extracted with ethyl acetate (3.0×2 liter) followed by filteration of the extract through celite bed and washing with ethyl acetate (1.0 liter). Combined extracts were dried over sodium sulfate and concentrated to yield a crude mass of 590 g. (Dark brown solid). This mass was used directly in step 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957083B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-fd146bc4dee84d3794b6b89f0e633711 |
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| Source note | uspto-grants-2015_02 |
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