HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784830Generated: October 30, 2026
Potassium Carbonate → 1-Bromo-3-iodo-5-(4-methoxy-benzyloxy)-benzene
https://huagongshe.com/reaction/1784830
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Reactant | 3-Bromo-5-iodophenol | HCID 22630182 | — |
| Catalyst | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 1-Bromo-3-iodo-5-(4-methoxy-benzyloxy)-benzene | HCID 50994026 | 77.8% |
Reaction Steps
3-Bromo-5-iodo-phenol (8.48 g, 28.37 mmol) was dissolved in DMF (50 mL) under dry argon and cooled to 0° C. Then potassium carbonate (3.92 g, 28.37 mmol) was added, followed by drop wise addition of 4-methoxybenzyl chloride (3.7 mL, 27.0 mmol). The mixture was slowly warmed to room temperature and stirred for 20 h. Additional 4-methoxybenzyl chloride (0.19 mL, 1.4 mmol) was added and the mixture was stirred for additional 24 h at room temperature. The reaction mixture was diluted with tert-butylmethyl ether (300 mL) and water (150 mL). The layers were separated and the aqueous one extracted with tert-butylmethyl ether (2×150 mL). The combined organics were washed with water and brine (150 mL), dried (Na2SO4) and concentrated to give the crude product which was purified by flash chromatography on silica gel (330 g, AcOEt/heptane 1:9). 1-Bromo-3-iodo-5-(4-methoxy-benzyloxy)-benzene (8.80 g, 59%, purity 80%, HPLC 220 nm) was obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504401B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-c5c30b34a447446bb1f71cc9561ce8c5 |
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| Source note | uspto-grants-2009_03 |
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