Water → 4-[2-Hydroxyadamant-1-yl-1-(imidazolyl)methyl]benzonitrile

HRID 35911

Reaction equation

HRID 35911 reaction equation
[NH:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH2:6][C:7]1[CH:14]=[CH:13][C:10]([C:11]#[N:12])=[CH:9][CH:8]=1.C([N-]C(C)C)(C)C.[Li+].[CH:23]12[CH2:32][CH:27]3[CH2:28][CH:29]([CH2:31][CH:25]([CH2:26]3)[C:24]1=[O:33])[CH2:30]2.O>O1CCCC1>[OH:33][CH:24]1[CH:23]2[CH2:32][CH:27]3[CH2:28][CH:29]([CH2:31][C:25]1([CH:6]([C:7]1[CH:14]=[CH:13][C:10]([C:11]#[N:12])=[CH:9][CH:8]=1)[C:2]1[NH:1][CH:5]=[CH:4][N:3]=1)[CH2:26]3)[CH2:30]2

Participants

6

Procedure

5.0 g of 4-[1-(imidazolyl)methyl]benzonitrile is dissolved in 100 ml of tetrahydrofuran and combined at -50° with 20 ml of 1.5-molar solution of lithium diisopropylamide in tetrahydrofuran, stirred for 0.5 hour at -60° combined With 4 3 g of 2-adamantanone, further stirred for 1 hour, and heated to 25°. Then water is added, the mixture is extracted three times with ethyl acetate, washed neutral with water, dried over sodium sulfate, and concentrated to dryness under vacuum, thus obtaining 6.66 g of crude 4-[2-hydroxy-adamant-1-yl-1-(imidazolyl)methyl]benzonitrile.

Workup

  1. stirringfurther stirred for 1 hour
  2. temperatureheated to 25°
  3. extractionthe mixture is extracted three times with ethyl acetate
  4. washwashed neutral with water
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated to dryness under vacuum

Sources & evidence

ORD record
ord-377e765bff1143e593a7d59d89ccb6b9
Source dataset
uspto-grants-1995_05
Patent number
US05411982

Linked notes

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