HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416964Generated: November 1, 2026
Hydrogen Bromide → 10-Bromo-1,1,1,2,2,3,3,4,4-nonafluorodecane
https://huagongshe.com/reaction/2416964
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 7,7,8,8,9,9,10,10,10-nonafluorodecan-1-ol | HCID 2775809 | — |
| Solvent | Water | HCID 962 | — |
| Product | 10-Bromo-1,1,1,2,2,3,3,4,4-nonafluorodecane | HCID 22630491 | — |
Reaction Steps
To a mixture of 18.00 g of 6-(nonafluorobutyl)-1-hexanol and 225 mL of 48 weight percent hydrobromic acid was slowly added 23 mL of concentrated sulfuric acid. The reaction mixture was heated at 100° C. for 12 hr and poured into 1 liter of water. The mixture was extracted with hexanes, and the combined organic phases were then washed with saturated aqueous sodium bicarbonate and dried over anhydrous magnesium sulfate. The hexanes solution was concentrated to a light amber liquid, which was eluted through 2 inches (5 cm) of silica with hexanes. Concentration of the eluent yielded a light amber liquid, and bulb-to-bulb distillation gave 18.29 g of 1-bromo-6-(nonafluorobutyl)hexane as a clear, colorless liquid, b.p. 70-80° C. at 0.05 torr (7 Pa).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06824882B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-38ce5a3ded8e446197f4b8471f0f548d |
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| Source note | uspto-grants-2004_11 |
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