HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301245Generated: November 2, 2026
Hydrogen Bromide → 4-(2-Bromoethyl)-1,2-difluorobenzene
https://huagongshe.com/reaction/2301245
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-(3,4-Difluorophenyl)ethan-1-ol | HCID 2758313 | — |
| Product | 4-(2-Bromoethyl)-1,2-difluorobenzene | HCID 15020053 | 81% |
Reaction Steps
17.59 g (111 mmol) of 2-(3,4-difluorophenyl)ethanol, 16 ml (137 mmol) of hydrogen bromide, 6.8 ml (234 mmol) of conc. sulfuric acid were added in the order, and the mixture was heated under reflux for 3 hrs. The reaction mixture was poured onto an ice-bath, an organic layer and an aqueous layer were separated, the aqueous layer was extracted with ether, the extract combined with the organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate, and dried over anhydrous magnesium sulfate. The solvent was distilled off, the solution condensed and purified by vacuum distillation to obtain 21.96 g (bp 68-70° C./2-4 Torr.) of oily product. The oily product was purified by column chromatography (elution solvent: hexane:ethyl acetate=3:1), the eluate was further purified by vacuum distillation to obtain 19.79 g of the title compound (81%, bp 73-75° C./4 Torr.) as oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06500503B2 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-ddae51dcc0024154a85edb69abd871f2 |
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| Source note | uspto-grants-2002_12 |
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