Water → HCID 10721188, compound

HRID 482369Notes

Reaction equation

HRID 482369 reaction equation
C([O:3][C:4](=O)[CH2:5][C:6]([C:26]1[CH:31]=[CH:30][C:29]([O:32][CH2:33][C:34]2[CH:43]=[CH:42][C:41]3[C:36](=[CH:37][CH:38]=[CH:39][CH:40]=3)[N:35]=2)=[CH:28][CH:27]=1)([C:8]1[CH:13]=[CH:12][C:11]([O:14][CH2:15][C:16]2[CH:25]=[CH:24][C:23]3[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=3)[N:17]=2)=[CH:10][CH:9]=1)[CH3:7])C.[H-].[H-].[H-].[H-].[Li+].[Al+3].O.[OH-].[Na+]>C1COCC1>[N:17]1[C:18]2[C:23](=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:24]=[CH:25][C:16]=1[CH2:15][O:14][C:11]1[CH:12]=[CH:13][C:8]([C:6]([C:26]2[CH:31]=[CH:30][C:29]([O:32][CH2:33][C:34]3[CH:43]=[CH:42][C:41]4[C:36](=[CH:37][CH:38]=[CH:39][CH:40]=4)[N:35]=3)=[CH:28][CH:27]=2)([CH3:7])[CH2:5][CH2:4][OH:3])=[CH:9][CH:10]=1

Participants

6

Procedure

To a 0° C. solution in THF (40 mL) of 3,3-bis(4-(2-quinolylmethoxy)phenyl)-butanoic acid ethyl ester (3.2 g , 5.5 mmol), prepared as in Example 13, was added slowly a solution of LiAlH4 (1.0M, 6 mL, 6.0 mmol). The mixture was stirred for 2 hours and water (15 mL) was added slowly followed by aqueous 1N NaOH. The reaction mixture was diluted with THF (20 mL) and the mixture was filtered through a celite pad. The filtrate was extracted with ether and the organic extract was washed with water and brine, dried over MgSO4, filtered, and concentrated in vacuo to provide 3,3-bis(4-(2-quinolylmethoxy)phenyl)butan-1-ol (2.4 g) as a pale yellow foam.

Workup

  1. filtrationthe mixture was filtered through a celite pad
  2. extractionThe filtrate was extracted with ether
  3. extractionthe organic extract
  4. washwas washed with water and brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-4e006650ce364e72862586e157f46e59
Source dataset
uspto-grants-1998_08
Patent number
US05795900

Reaction notes

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