Acetone → ACMC-20apjz

HRID 261912

反応式

HRID 261912 の反応式
Br[CH:2]1[CH2:6][C:5](=[O:7])[C:4]([CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([OH:16])=[O:15])=[CH:3]1.CC(C)=[O:19]>[B-](F)(F)(F)F.[Ag+].O>[C:14]([CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][C:4]1[C:5](=[O:7])[CH2:6][CH:2]([OH:19])[CH:3]=1)([OH:16])=[O:15]

参加物

5

反応物 2

HCID 180AcetoneHCID 130462774-Bromo-2-(6-carboxyhexyl)cyclopent-2-en-1-one

生成物 1

HCID 3690897ACMC-20apjz

試薬・触媒・溶媒 2

HCID 159722Silver tetrafluoroborate触媒HCID 962Water溶媒

実験手順

To a stirred solution of 10.6 g. (ca. 34 mmoles) of crude 4-bromo-2-(6-carboxyhexyl)cyclopent-2-en-1-one (Example 8) in 100 ml. of acetone and 65 ml. of water is added 8.0 g. (45.2 mmoles) of silver fluoborate during 2 minutes. The temperature is maintained at 25°-30° C. by external cooling. The mixture is stirred for 90 minutes, filtered, saturated with sodium chloride and extracted with half saturated sodium bicarbonate solution. The basic extract is reacidified with dilute hydrochloric acid, saturated with sodium chloride, and extracted with ether. The extract is washed with water and saturated sodium chloride solution, dried over magnesium sulfate, and concentrated. The crude product is purified by partition chromatography on Celite to give an oil with the properties described in Example 27.

後処理

  1. temperatureThe temperature is maintained at 25°-30° C. by external cooling
  2. filtrationfiltered, saturated with sodium chloride
  3. extractionextracted with half saturated sodium bicarbonate solution
  4. extractionThe basic extract
  5. extractionextracted with ether
  6. washThe extract is washed with water and saturated sodium chloride solution
  7. dry with materialdried over magnesium sulfate
  8. concentrationconcentrated
  9. customThe crude product is purified
  10. customby partition chromatography on Celite
  11. customto give an oil with the properties

出典と根拠

ORDレコード
ord-fe90540513ff4433ae35360fde338743
出典データセット
uspto-grants-1979_05
特許番号
US04152524

関連ノート

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