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Water → 6-Chloroundecane

HRID 23801
Notes
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Reaction equation

HRID 23801 reaction equation
CS(O[CH:6]([CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])(=O)=O.[Cl-:17].[Li+].O>CN(C)C=O>[Cl:17][CH:6]([CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 962WaterHCID 433294Lithium ChlorideHCID 225905206-Methanesulfonyloxyundecane

Product 1

HCID 99206036-ChloroundecaneYield 97.1%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
15 °C

Procedure

Thirty grams (0.12 mol) of 6-methanesulfonyloxyundecane was dissolved in 150 mL of N,N-dimethylformamide and 15.3 g (0.36 mol) of anhydrous lithium chloride was added to the solution under cooling with ice. The mixture was warmed to 50˜55° C. and stirred for 3 hours. Thereafter, the mixture was cooled to 15° C. and 300 mL of cold water was added. The reaction mixture was extracted three times with 150 mL of hexane and the organic layer was sequentially washed with 150 mL of water and 150 mL of a saturated aqueous solution of sodium chloride and thereafter dried over 6 g of anhydrous magnesium sulfate. After filtering off the anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure to give 22.2 g (97.1% in yield) of 6-chloroundecane.

Workup

  1. temperatureunder cooling with ice
  2. temperatureThe mixture was warmed to 50˜55° C.
  3. extractionThe reaction mixture was extracted three times with 150 mL of hexane
  4. washthe organic layer was sequentially washed with 150 mL of water and 150 mL of a saturated aqueous solution of sodium chloride
  5. dry with materialdried over 6 g of anhydrous magnesium sulfate
  6. filtrationAfter filtering off the anhydrous magnesium sulfate
  7. distillationthe solvent was distilled off under reduced pressure

Sources & evidence

ORD record
ord-552f94c5b02243eb9ca1115a3c9d097d
Source dataset
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06852867B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes