6-Aminohexanoic Acid → HCID 86196164, compound

HRID 732866Notes

Reaction equation

HRID 732866 reaction equation
[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]([OH:9])=[O:8].[OH-].[Na+].C([O:16][C:17](OC(OC(C)(C)C)=O)=[O:18])(C)(C)C.O.[C:28](O)([CH3:31])([CH3:30])[CH3:29]>>[C:7]([CH2:6][CH2:5][CH2:4][CH2:3][CH:2]([NH2:1])[C:17]([OH:18])=[O:16])([O:9][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:8]

Participants

6

Procedure

6-Aminocaproic acid (10 g, 76 mmo) was dissolved in tert-butylalcohol (100 ml), 5N NaOH (15 ml, 76 mmol) was added thereto, and the mixture was stirred at room temperature for 10 minutes. Di-tert-butyl-dicarbonate (18.3 g, 83 mmol) dissolved in tert-butylalcohol (100 ml) was added thereto and stirred at room temperature for 24 hours. Then, water (100 ml) was added thereto and the mixture was concentrated under a reduced pressure, cooled to 0° C., and then, 2N H2SO4 was added thereto dropwise until pH of the mixture became 2. Thereafter, the resultant was extracted with ethyl acetate, the extract was washed with water, dried over MgSO4 and concentrated. The concentrate was purified using column chromatography (ethyl acetate:toluene:acetic acid=20:10:0.3) to obtain the title compound (17.9 g) as a white solid.

Workup

  1. additionwas added
  2. stirringstirred at room temperature for 24 hours
  3. concentrationthe mixture was concentrated under a reduced pressure
  4. temperaturecooled to 0° C.
  5. addition2N H2SO4 was added
  6. extractionThereafter, the resultant was extracted with ethyl acetate
  7. washthe extract was washed with water
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated
  10. customThe concentrate was purified

Sources & evidence

ORD record
ord-cc54cb5847964cdfb4d9aa02ddb8d7c3
Source dataset
uspto-grants-2009_09
Patent number
US07589072B2

Reaction notes

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