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Water → (4S)-2,2-Dimethyl-4-(4-cyanophenoxy)methyl-1,3-dioxolane

HRID 466220
ノート
印刷プレビュー

反応式

HRID 466220 の反応式
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1.[OH-:10].[K+].[OH2:12]>CO>[CH3:3][C:2]1([CH3:9])[O:12][C@@H:5]([CH2:6][O:1][C:2]2[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=2)[CH2:4][O:10]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 130194-CyanophenolHCID 14797Potassium Hydroxide

生成物 1

HCID 15066863(4S)-2,2-Dimethyl-4-(4-cyanophenoxy)methyl-1,3-dioxolane

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
110 °C

実験手順

A solution of 4-hydroxy benzonitrile (55 g) in methanol (100 ml) was treated with potassium hydroxide (29 g) in water (30 ml) and evaporated at reduced pressure. The remaining potassium salt was dissolved in dry dimethylformamide (75 ml) and (4R)-2,2-dimethyl-4 - methanesulfonyloxymethyl-1,3-dioxolane, 82.2 g, was add stirring at 110° C. for 20 h, allowed to cool and distributed between ether and water. The aqueous phase was extracted three times with ether, the combined ether phases washed three times with 10% aqueous potassium hydroxide and twice with water, dried over anhydrous sodium sulfate and evaporated. Yield 77 g of the title compound.

後処理

  1. customevaporated at reduced pressure
  2. dissolutionThe remaining potassium salt was dissolved in dry dimethylformamide (75 ml)
  3. addition(4R)-2,2-dimethyl-4 - methanesulfonyloxymethyl-1,3-dioxolane, 82.2 g, was add
  4. temperatureto cool
  5. extractionThe aqueous phase was extracted three times with ether
  6. washthe combined ether phases washed three times with 10% aqueous potassium hydroxide
  7. dry with materialtwice with water, dried over anhydrous sodium sulfate
  8. customevaporated

出典と根拠

ORDレコード
ord-104d16223d4a4b9ca9b898b2d5970fa2
出典データセット
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05155133

反応ノート

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