HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394998Generated: October 29, 2026
1,2-Dibromoethane → HCID 22471323, compound
https://huagongshe.com/reaction/394998
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,4-Difluorophenol | HCID 75927 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22471323 | HCID 22471323 | — |
Reaction Steps
A mixture of 15 g of 3,4-difluorophenol, 23.5 g of potassium carbonate and 60 cm3 of 1,2-dibromoethane in 250 cm3 of acetonitrile was stirred at a temperature in the region of 70° C. for 18 hours. After cooling to about 20° C., the reaction mixture was filtered through Celite and then concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40° C. The residue obtained was purified by chromatography under atmospheric pressure, on a column of silica gel (particle size 70-200μ; diameter 8 cm; mass 400 g), eluting with 40-60° C. petroleum ether. The fractions containing the product were combined and then concentrated to dryness under reduced pressure (2 kPa) in the region of 40° C. 15.7 g of 4-(2-bromoethoxy)-1,2-difluorobenzene were obtained in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06603005B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-bd1af2eef62c44f3a6468a8a9e3c366b |
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| Source note | uspto-grants-2003_08 |
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