4-Fluoroanisole → (2-Fluoro-5-methoxy-phenyl)-4-pyridylmethanol

HRID 273735

反応式

HRID 273735 の反応式
C([Li])CCC.CN(C)CCN(C)CCN(C)C.[F:18][C:19]1[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[CH:21][CH:20]=1.[N:27]1[CH:32]=[CH:31][C:30]([CH:33]=[O:34])=[CH:29][CH:28]=1>C1COCC1>[F:18][C:19]1[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[CH:21][C:20]=1[CH:33]([C:30]1[CH:31]=[CH:32][N:27]=[CH:28][CH:29]=1)[OH:34]

参加物

6

反応物 4

HCID 99874-FluoroanisoleHCID 133894-PyridinecarboxaldehydeHCID 18196PentamethyldiethylenetriamineHCID 178418339Butyllithium

生成物 1

HCID 15839523(2-Fluoro-5-methoxy-phenyl)-4-pyridylmethanol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-75 °C

実験手順

Butyl lithium (47.5 ml of 2.22M solution, 105.6 mmole) was added slowly to a solution of pentamethyldiethylenetriamine (15 ml) and 4-fluoroanisole (12.61 g, 0.1 mole) in THF (150 ml) at -70° C. The solution was stirred for 2 hr at -75° C. and a solution of pyridine-4-aldehyde (9.55 ml, 0.1 mole) in THF was added at -75° C. The mixture was allowed to warm to 25° C. slowly and then quenched with ammonium chloride solution. The mixture was diluted with ethyl acetate and the organic layer was separated. The organic layer was washed with water and 3N hydrochloric acid. The acid washes were then basified with sodium hydroxide and extracted with ether and the ether solution concentrated in vacuo. The crude product was recrystallized from 80% ethanol to give (2-fluoro-5-methoxy-phenyl)-4-pyridylmethanol as a white powder (12.22 g+3.12 g second crop, 65.8% total yield).

後処理

  1. temperatureto warm to 25° C. slowly
  2. customquenched with ammonium chloride solution
  3. additionThe mixture was diluted with ethyl acetate
  4. customthe organic layer was separated
  5. washThe organic layer was washed with water and 3N hydrochloric acid
  6. extractionextracted with ether
  7. concentrationthe ether solution concentrated in vacuo
  8. customThe crude product was recrystallized from 80% ethanol
  9. customto give

出典と根拠

ORDレコード
ord-9e5b4049d4ec4d8581fdf77a8058c374
出典データセット
uspto-grants-1995_02
特許番号
US05387593

関連ノート

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