HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399239Generated: October 29, 2026
Potassium Carbonate → 1-Bromo-2-(2-benzyloxyeth-1-yloxy)-4-methoxybenzene
https://huagongshe.com/reaction/399239
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, ((2-bromoethoxy)methyl)- | HCID 73833 | — |
| Reactant | 2-Bromo-5-methoxyphenol | HCID 13493839 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Bromo-2-(2-benzyloxyeth-1-yloxy)-4-methoxybenzene | HCID 18427680 | 83% |
Reaction Steps
A mixture of 1-bromo-2-hydroxy-4-methoxy benzene (68.3 g, 0.336 moles), anhydrous potassium carbonate (51.2 g 0.37 moles) and 0.5 L of N,N-dimethylformamide was heated to 65° C. Benzyloxyethylbromide (76.0 g, 0.353 moles) was added dropwise over 0.5 hr. After stirring for 1.5 hr. at 65° C., the reaction mixture was cooled and filtered. The filtrate was diluted with 1 L of deionized water, and extracted with 3×0.5 L ethyl acetate. The organic extracts were washed with brine, dried over MgSO4, and concentrated in vacuo. Distillation gave 93 g (83%) of product as a yellow liquid (b.p. 170°-175° C., 0.5 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05817693 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-2c474371371a41bf9a886b3a6f230217 |
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| Source note | uspto-grants-1998_10 |
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