Water → HCID 19366809, compound

HRID 849535Notes

Reaction equation

HRID 849535 reaction equation
C[CH:2]([CH:6]([S:12]([C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1)(=[O:14])=[O:13])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])[C:3](O)=[O:4].[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>C1COCC1>[CH3:22][O:21][C:18]1[CH:17]=[CH:16][C:15]([S:12]([CH:6]([CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])[CH2:2][CH2:3][OH:4])(=[O:13])=[O:14])=[CH:20][CH:19]=1

Participants

6

Procedure

Part C: To a solution of 4.4 g (13 mmol) of methyl 3-[(4-methoxyphenyl)sulfonyl]-octanoic acid from Part B in 60 mL of anhydrous THF at zero° C. under nitrogen, was added 14.6 mL (0.5 g, 13 mmol) of a 1.0 M solution of lithium aluminum hydride in THF. After 2 hours, the reaction mixture was cooled to zero° C. and 0.5 mL of water was added, followed by 0.5 mL of 2.5 N sodium hydroxide solution and 1.5 mL of water, the reaction was filtered, the filtrate concentrated in vacuo, ethyl acetate and 5% citric acid solution were added, the organic layer was separated and washed with saturated sodium bicarbonate solution and brine, dried with magnesium sulfate, filtered and concentrated to afford 3.3 grams of pure 3-[(4-methoxyphenyl)sulfonyl]-octan-1-ol, m/z=307 (M+Li).

Workup

  1. temperaturethe reaction mixture was cooled
  2. filtrationthe reaction was filtered
  3. concentrationthe filtrate concentrated in vacuo, ethyl acetate and 5% citric acid solution
  4. additionwere added
  5. customthe organic layer was separated
  6. washwashed with saturated sodium bicarbonate solution and brine
  7. dry with materialdried with magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-56548d52a78442438006ed599a14c4ac
Source dataset
uspto-grants-2000_01
Patent number
US06013649

Reaction notes

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