HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496033Generated: October 30, 2026
2-Bromoethanol → 2-(3,4-Dimethoxyphenoxy)ethanol
https://huagongshe.com/reaction/496033
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,4-Dimethoxyphenol | HCID 16251 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(3,4-Dimethoxyphenoxy)ethanol | HCID 12298883 | 60% |
Reaction Steps
K2CO3 (1.07 g, 7.78 mmol) was added to a solution of 3,4,dimethoxyphenol (1.0 g, 6.48 mmol) in dry DMF (15 ml). 2-Bromoethanol (0.81 g, 6.48 mmol) was added, and the mixture was heated overnight at 120° C. The mixture was cooled, taken up in EtOAc, extracted with water (20 ml), saturated NaCl (4×20 ml), dried over MgSO4, and evaporated under reduced pressure. The product was purified by column chromatography on silica (Hexane:EtOAc 3:1) to give the desired product in 60% yield. B. Synthesis of 4-(2-bromo-ethoxy)-1,2-dimethoxy benzene
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06943168B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-ea5b61dfd50746b4b6f1e99a6c33b1e7 |
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| Source note | uspto-grants-2005_09 |
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