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Ethylene Glycol → 3-Fluoro-4-(2-hydroxyethoxy)benzonitrile

HRID 2078427
ノート
印刷プレビュー

反応式

HRID 2078427 の反応式
CC(C)([O-])C.[K+].[F:7][C:8]1[CH:9]=[C:10]([CH:13]=[CH:14][C:15]=1F)[C:11]#[N:12].[CH2:17]([OH:20])[CH2:18][OH:19]>>[F:7][C:8]1[CH:9]=[C:10]([CH:13]=[CH:14][C:15]=1[O:19][CH2:18][CH2:17][OH:20])[C:11]#[N:12]
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

4

反応物 3

HCID 174Ethylene GlycolHCID 5872033,4-DifluorobenzonitrileHCID 23665647Potassium tert-butoxide

生成物 1

HCID 436574753-Fluoro-4-(2-hydroxyethoxy)benzonitrile収率 100%

反応条件

温度
50 °C

実験手順

To potassium tert-butoxide (19.35 g) was added ethylene glycol (160 mL). The mixture was then heated to 50° C. At 50° C., 3,4-difluorobenzonitrile (20 g) was added and this was washed in with ethylene glycol (40 mL). The combined solution was heated to 80° C., and held at this temperature for two hours, before being cooled to 20° C. over one hour. The reaction mixture was filtered and washed with ethylene glycol (40 mL). To the filtrate was added water (200 mL) and dichloromethane (200 mL). The layers were separated and the organic layer was concentrated in vacuo, to give the sub-title compound as a waxy white solid (26.1 g, 100% yield).

後処理

  1. washthis was washed in with ethylene glycol (40 mL)
  2. temperatureThe combined solution was heated to 80° C.
  3. temperaturebefore being cooled to 20° C. over one hour
  4. filtrationThe reaction mixture was filtered
  5. washwashed with ethylene glycol (40 mL)
  6. additionTo the filtrate was added water (200 mL) and dichloromethane (200 mL)
  7. customThe layers were separated
  8. concentrationthe organic layer was concentrated in vacuo

出典と根拠

ORDレコード
ord-f69f4b67b47c4aa4a1b4ecb53780308a
出典データセット
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07928225B2

反応ノート

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