Water → HCID 178509701、化合物

HRID 1198182ノート

反応式

HRID 1198182 の反応式
[NH:1]1[CH:5]=[C:4]([CH2:6][C:7]2[CH:14]=[CH:13][C:10]([C:11]#[N:12])=[CH:9][CH:8]=2)[N:3]=[N:2]1.C([N-]C(C)C)(C)C.[Li+].[C:23]1(=[O:28])[CH2:27][CH2:26][CH2:25][CH2:24]1.O>O1CCCC1>[OH:28][C:23]1([CH:6]([C:7]2[CH:14]=[CH:13][C:10]([C:11]#[N:12])=[CH:9][CH:8]=2)[C:4]2[N:3]=[N:2][NH:1][CH:5]=2)[CH2:27][CH2:26][CH2:25][CH2:24]1

参加物

6

反応物 4

HCID 962WaterHCID 8452CyclopentanoneHCID 2724682Lithium diisopropylamideHCID 1785097034-[1-(1,2,3-Triazolyl)methyl]-benzonitrile

生成物 1

HCID 178509701HCID 178509701、化合物収率 97.5%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

5 g of 4-[1-(1,2,3-triazolyl)methyl]benzonitrile is dissolved in 100 ml of tetrahydrofuran and combined at -60° with 20 ml of 1.5-molar solution of lithium diisopropylamide in tetrahydrofuran, stirred for 0.5 hour, further stirred for 1 hour at -70° with 2.4 g of cyclopentanone, and heated to 25°. Then the mixture is combined with water, extracted three times with ethyl acetate, washed with water, dried over sodium sulfate, and concentrated to dryness under vacuum, thus obtaining 7.1 g of crude 4-[1-hydroxycyclopent-1-yl-1-(1,2,3-triazolyl)methyl]benzonitrile.

後処理

  1. temperatureheated to 25°
  2. extractionextracted three times with ethyl acetate
  3. washwashed with water
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated to dryness under vacuum

出典と根拠

ORDレコード
ord-4c7e936ff6e54d63bed6e1157674481f
出典データセット
uspto-grants-1994_01
特許番号
US05280035

反応ノート

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