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Potassium Carbonate → 4-Formyl-3-hydroxybenzonitrile

HRID 343938
ノート
印刷プレビュー

反応式

HRID 343938 の反応式
[C:1]([C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[O:8])=[C:5](F)[CH:4]=1)#[N:2].C(=O)([O-])[O-:13].[K+].[K+]>CN(C)C=O.O>[C:1]([C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[O:8])=[C:5]([OH:13])[CH:4]=1)#[N:2]
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 2

HCID 11430Potassium CarbonateHCID 27831503-Fluoro-4-formylbenzonitrile

生成物 1

HCID 128136484-Formyl-3-hydroxybenzonitrile

試薬・触媒・溶媒 2

HCID 962Water溶媒5 回HCID 6228Dimethylformamide溶媒

反応条件

温度
90 °C

実験手順

A mixture of 4-cyano-2-fluorobenzaldehyde (11.73 g, 78.7 mmol) and potassium carbonate (14.12 g, 102.3 mmol) was dissolved in dry dimethylformamide (35 ml). To this was added water (6.63 ml, 368.5 mmol). The resulting solution was heated to 90° C. with stirring. A further equivalent of water (1.42 ml) was added after 2 hours, then a further two equivalents of water (2.84 ml) 1 hour later. The resulting solution was left overnight. After 24 hours a further 2 equivalents of water (2.84 ml) was added, then heated for a further 2 hours at 90° C. The cooled solution was diluted with water to form a murky yellow solution. The solid precipitate was filtered. The remaining yellow filtrate was acidified with concentrated hydrochloric acid to produce a yellow solid. This was filtered, then dried at 40° C. overnight to give 4-cyano-2-hydroxybenzaldehyde as a yellow solid.

後処理

  1. temperatureheated for a further 2 hours at 90° C
  2. customto form a murky yellow solution
  3. filtrationThe solid precipitate was filtered
  4. customto produce a yellow solid
  5. filtrationThis was filtered
  6. customdried at 40° C. overnight

出典と根拠

ORDレコード
ord-d5f4aa2c2b6f46cca0dba9f9d239f44a
出典データセット
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05863947

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート