HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880259Generated: October 31, 2026
Water → 5-Bromo-1,3-dichloro-2-(difluoromethoxy)benzene
https://huagongshe.com/reaction/1880259
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromo-2,6-dichlorophenol | HCID 18587 | — |
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-Bromo-1,3-dichloro-2-(difluoromethoxy)benzene | HCID 66865742 | — |
Reaction Steps
To a solution of 2.3 g of 4-bromo-2,6-dichlorophenol in 25 mL of acetonitrile, 1.3 g of potassium carbonate and 3.8 g of ethyl bromodifluoroacetate were added and the resultant mixture was stirred while heating the mixture to reflux for 4 hours. After the completion of the reaction, the reaction mixture was left to be cooled down to room temperature and charged into 100 mL of water and the resultant mixture was extracted with ethyl acetate (100 mL×1). The organic phase was washed with water and then dehydrated and dried over saturated saline and anhydrous sodium sulfate in this order and the solvent was distilled off under reduced pressure. The resultant residue was purified by silica gel column chromatography eluting with ethyl acetate-hexane (1:4) to obtain 2.4 g of the objective substance as a yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318757B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-5d402632bb754b91a7fd1c6bc7b238ba |
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| Source note | uspto-grants-2012_11 |
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