HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773969Generated: November 2, 2026
Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) → 4-Bromo-2-chloro-1-(2-chloroethoxy)benzene
https://huagongshe.com/reaction/1773969
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol, 2-chloro-, 1-(4-methylbenzenesulfonate) | HCID 6639 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-2-chlorophenol | HCID 19859 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Bromo-2-chloro-1-(2-chloroethoxy)benzene | HCID 43135623 | — |
Reaction Steps
Potassium carbonate (8.29 g, 60 mmol, 3.0 eq.) and 2-chloroethyl p-toluenesulfonate (5.16 g, 22 mmol, 1.1 eq.) were added in sequence to a solution of 4-bromo-2-chlorophenol (4.19 g, 20 mmol, 1.0 eq.) in DMF (25 mL). The resulting mixture was heated up to 60° C. and stirred at that temperature for 4 hours. The mixture was allowed to cool down to r.t. and was partitioned between AcOEt (290 mL) and water (120 mL). The layers were separated. The org. phase was washed with water (4×120 mL), dried over MgSO4, filtered, and concentrated in vacuo to give 4-bromo-2-chloro-1-(2-chloro-ethoxy)-benzene as a colorless oil that solidified upon standing. The product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09255090B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-e97a8e7e3c734083a67b37c694b84edd |
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| Source note | uspto-grants-2016_02 |
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