Sulfuric Acid → HCID 21270603, compound

HRID 1193862Notes

Reaction equation

HRID 1193862 reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].CC[O:9]CC.[CH2:12]([CH:18]([CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[CH2:19][O:20][CH2:21][C:22](O)=O)[CH2:13][CH2:14][CH2:15][CH2:16][CH3:17].OS(O)(=O)=O>O>[CH2:12]([CH:18]([CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH3:32])[CH2:19][O:20][CH:21]([OH:9])[CH3:22])[CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]

Participants

6

Procedure

In a three-necked, one-liter, round-bottom flask (equipped with a reflux condenser, nitrogen inlet, dropping funnel, and magnetic stirring bar) 0.15 mole of lithium aluminum hydride was dispersed in 300 ml. of ether at room temperature and under a dry nitrogen atmosphere. The 2-hexyldecyloxyacetic acid from Part A was mixed with 200 ml. of ether and added dropwise with stirring. The resulting mixture was stirred overnight at room temperature. The flask containing the mixture was then cooled in ice, and icecold water was added dropwise to the mixture to react with any excess reducing agents. The reaction mixture was acidified with 10% H2SO4 to a pH of one, and extracted with 300 ml. of ether twice. The ether layers from the two extractions were diluted with an equal volume of water, and washed two times with saturated NaHC3 solution. The mixture was then washed with water and dried with anhydrous magnesium sulfate. 2-hexyldecyloxyethanol was obtained after removing the ether.

Workup

  1. customat room temperature
  2. stirringThe resulting mixture was stirred overnight at room temperature
  3. additionThe flask containing the mixture
  4. temperaturewas then cooled in ice
  5. customto react with
  6. extractionextracted with 300 ml
  7. extractionThe ether layers from the two extractions
  8. additionwere diluted with an equal volume of water
  9. washwashed two times with saturated NaHC3 solution
  10. washThe mixture was then washed with water
  11. dry with materialdried with anhydrous magnesium sulfate

Sources & evidence

ORD record
ord-30133814972b48e8a73884600d47ff88
Source dataset
uspto-grants-1989_03
Patent number
US04811788

Reaction notes

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