1-Iodohexane → HCID 14986433, compound

HRID 1494258Notes

Reaction equation

HRID 1494258 reaction equation
[OH:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][O:15][C:16]1[CH:24]=[CH:23][C:19]([C:20]([OH:22])=[O:21])=[C:18]([OH:25])[C:17]=1[CH2:26][CH2:27][CH3:28].[CH2:29](I)[CH2:30][CH2:31][CH2:32][CH2:33][CH3:34].C(=O)(O)[O-].[Na+]>CN(C)C=O>[CH2:29]([O:21][C:20](=[O:22])[C:19]1[CH:23]=[CH:24][C:16]([O:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][C:3]2[CH:4]=[CH:5][CH:6]=[C:7]([OH:8])[C:2]=2[OH:1])=[C:17]([CH2:26][CH2:27][CH3:28])[C:18]=1[OH:25])[CH2:30][CH2:31][CH2:32][CH2:33][CH3:34]

Participants

5

Procedure

A mixture of 1.00 g (2.57 mmol) of 4-[6-(2,3-dihydroxyphenyl)hexyloxy]-2-hydroxy-3-propylbenzoic acid, 0.76 mL (5.15 mmol) of n-hexyl iodide and 0.26 g (3.36 mmol) of sodium bicarbonate in 15 mL of anhydrous dimethylformamide was stirred and heated at 70° for 16 hours. The solvent was removed on the oil pump, water was added and the product was extracted with ethyl acetate. The dried extract was concentrated under reduced pressure to an oil which was purified by chromatography on silica gel using 5% ethyl acetate-toluene to give 1.01 g (83% yield) of 4-[6-(2,3-dihydroxyphenyl)hexyloxy]-2-hydroxy-3-propylbenzoic acid hexyl ester as an oil.

Workup

  1. temperatureheated at 70° for 16 hours
  2. customThe solvent was removed on the oil pump, water
  3. additionwas added
  4. extractionthe product was extracted with ethyl acetate
  5. extractionThe dried extract
  6. concentrationwas concentrated under reduced pressure to an oil which
  7. customwas purified by chromatography on silica gel using 5% ethyl acetate-toluene

Sources & evidence

ORD record
ord-af645146e1bb4e5987d6eff72767c4ac
Source dataset
uspto-grants-1991_06
Patent number
US05025036

Reaction notes

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