HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990739Generated: October 29, 2026
Chlorodifluoromethane → 1-Bromo-3-(difluoromethoxy)-5-fluorobenzene
https://huagongshe.com/reaction/1990739
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorodifluoromethane | HCID 6372 | — |
| Reactant | 3-Bromo-5-fluorophenol | HCID 21904636 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 1-Bromo-3-(difluoromethoxy)-5-fluorobenzene | HCID 21904622 | 81.6% |
Reaction Steps
A mixture of 3-bromo-5-fluorophenol (6.1 g, 31.0 mmol; see step (ii) above) and chlorodifluoromethane (13.0 g, 150.0 mmol) in i-PrOH (100 mL) and 30% KOH (80 mL) was heated in a sealed flask for 18 h at 80-85° C. The reaction mixture was cooled to room temperature and the layers were separated. The organic layer was concentrated in vacuo to afford a colourless oil. The aqueous layer was extracted with Et2O (3× 30 mL). The crude oil and the combined organic extracts were washed with 2N NaOH (3× 30 mL) and H2O (3× 30 mL). The organics were then dried (Na2SO4), filtered through a small silica gel plug, and concentrated in vacuo to afford the sub-title compound (6.1 g, 79%) as a colourless oil that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07645751B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-9d9385364060452f83215b17ba395d9c |
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| Source note | uspto-grants-2010_01 |
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