Sodium Hydroxide → HCID 14327319, compound

HRID 704360Notes

Reaction equation

HRID 704360 reaction equation
[N:1]1([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][O:11][C:12]2[CH:13]=[C:14]([CH:28]=[CH:29][CH:30]=2)[O:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]([CH3:27])([CH3:26])[C:21]([O:23]CC)=[O:22])[CH:5]=[CH:4][N:3]=[CH:2]1.[OH-].[Na+]>C(O)C>[N:1]1([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][O:11][C:12]2[CH:13]=[C:14]([CH:28]=[CH:29][CH:30]=2)[O:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]([CH3:26])([CH3:27])[C:21]([OH:23])=[O:22])[CH:5]=[CH:4][N:3]=[CH:2]1

Participants

4

Procedure

A mixture of 3.5 g ethyl 6-[m-[5-(1-imidazolyl)pentyloxy]phenoxy]-2,2-dimethylhexanoate, 20 ml of 1N NaOH solution and 20 ml ethanol was heated under reflux overnight. Ethanol was distilled off under reduced pressure, and concentrated hydrochloric acid was added to the remaining aqueous soluiton to lower its pH down to about 4.0. The pasty solid which separated out was extracted with chloroform, and the extract was washed with water and dried. The solvent was ditilled off, and the crude product thus obtained was purified by silica gel column chromatography, affording 3.2 g of 6-[m-[5-(1-imidazolyl)pentyloxy]phenoxy]-2,2-dimethylhexanoic acid.

Workup

  1. temperaturewas heated
  2. temperatureunder reflux overnight
  3. distillationEthanol was distilled off under reduced pressure, and concentrated hydrochloric acid
  4. additionwas added to the remaining aqueous soluiton
  5. customThe pasty solid which separated out
  6. extractionwas extracted with chloroform
  7. washthe extract was washed with water
  8. customdried
  9. customthe crude product thus obtained
  10. customwas purified by silica gel column chromatography

Sources & evidence

ORD record
ord-c284375547b24b668022f6fdd87043ec
Source dataset
uspto-grants-1991_01
Patent number
US04987147

Reaction notes

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