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Hydrogen Bromide → 8-Bromo-1,1,1,2,2,3,3,4,4-nonafluorooctane

HRID 2416967
Notes
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Reaction equation

HRID 2416967 reaction equation
[F:1][C:2]([F:18])([C:14]([F:17])([F:16])[F:15])[C:3]([F:13])([F:12])[C:4]([F:11])([F:10])[CH2:5][CH2:6][CH2:7][CH2:8]O.[BrH:19].S(=O)(=O)(O)O>O>[Br:19][CH2:8][CH2:7][CH2:6][CH2:5][C:4]([F:11])([F:10])[C:3]([F:13])([F:12])[C:2]([F:18])([F:1])[C:14]([F:17])([F:16])[F:15]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 260Hydrogen BromideHCID 1118Sulfuric AcidHCID 27696614:4 Fluorotelomer alcohol

Product 1

HCID 155453038-Bromo-1,1,1,2,2,3,3,4,4-nonafluorooctane

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
100 °C

Procedure

To a mixture of 12.50 g of 4-(nonafluorobutyl)-1-butanol and 150 mL of 48 weight percent hydrobromic acid was slowly added 15 mL of concentrated sulfuric acid. The reaction mixture was heated at 100° C. for 18 hr, and then poured into 500 mL of water. The mixture was extracted with hexanes, and the combined organic phases were washed with saturated aqueous sodium bicarbonate and dried over anhydrous magnesium sulfate. Filtration and concentration afforded 12.50 g of crude 1-bromo-4-(nonafluorobutyl)butane as a light amber liquid, which was used without further purification.

Workup

  1. extractionThe mixture was extracted with hexanes
  2. washthe combined organic phases were washed with saturated aqueous sodium bicarbonate
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationFiltration and concentration

Sources & evidence

ORD record
ord-d8cbbb63dd80474ca535eb1ea2f18cdd
Source dataset
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06824882B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes