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Potassium Acetate → 3-Cyclopentylbicyclo[3.2.0]hept-3-en-6-one

HRID 551656
ノート
印刷プレビュー

反応式

HRID 551656 の反応式
C([O-])(=O)C.[K+].O[CH:7]([CH:12]([CH:16]1[CH2:20][CH2:19][CH2:18][CH2:17]1)[CH2:13][CH:14]=[CH2:15])[CH2:8][C:9]([OH:11])=O>C(OC(=O)C)(=O)C>[CH:16]1([C:12]2[CH2:13][CH:14]3[CH:8]([CH:7]=2)[C:9](=[O:11])[CH2:15]3)[CH2:20][CH2:19][CH2:18][CH2:17]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 517044Potassium AcetateHCID 67198011HCID 67198011、化合物

生成物 1

HCID 671994463-Cyclopentylbicyclo[3.2.0]hept-3-en-6-one

試薬・触媒・溶媒 1

HCID 7918Acetic Anhydride溶媒

実験手順

Potassium acetate (4.16 g, 42.4 mmol) was added to an acetic anhydride (20 mL) solution of 3-hydroxy-4-cyclopentylhept-6-enoic acid (4.00 g, 17.7 mmol at the maximum), and the mixture was stirred at room temperature for 1 hour and then stirred at 120° C. for 3.5 hours. The mixture was treated with ice water, followed by extraction with diethyl ether. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate. The organic layer was dried over anhydrous magnesium sulfate. Then, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography to obtain the compound of interest as a yellow oil substance (2.30 g, 74%).

後処理

  1. stirringstirred at 120° C. for 3.5 hours
  2. extractionfollowed by extraction with diethyl ether
  3. washThe organic layer was washed with a saturated aqueous solution of sodium bicarbonate
  4. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  5. distillationThen, the solvent was distilled off under reduced pressure
  6. customthe residue was purified by silica gel column chromatography
  7. customto obtain the compound of interest as a yellow oil substance (2.30 g, 74%)

出典と根拠

ORDレコード
ord-e676a1dede5542dd88888f1dabfdc113
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07947738B2

反応ノート

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