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Diethyl Ether → 5-hydroxy-4-(hydroxymethyl)hexahydro-2H-cyclopenta[b]furan-2-one

HRID 1797432
ノート
印刷プレビュー

反応式

HRID 1797432 の反応式
C([O:4][CH:5]1[CH2:13][CH:8]2[O:9][C:10](=[O:12])[CH2:11][CH:7]2[CH:6]1[CH2:14][O:15]C(=O)C)(=O)C.C(=O)([O-])[O-].[K+].[K+].C(OCC)(=O)C.C(OCC)C>CO>[OH:4][CH:5]1[CH2:13][CH:8]2[O:9][C:10](=[O:12])[CH2:11][CH:7]2[CH:6]1[CH2:14][OH:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 3283Diethyl EtherHCID 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 494700HCID 494700、化合物

生成物 1

HCID 37592585-hydroxy-4-(hydroxymethyl)hexahydro-2H-cyclopenta[b]furan-2-one収率 54%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

To a solution of 50 (10.0 g, 39 mmol) in MeOH (100 mL) was added potassium carbonate (15 g). The suspension was stirred at room temperature for 3 hours. To the suspension was added ethyl acetate (60 mL). The resulting suspension was filtered through a pad of diatomaceous earth (Celite®). The filtrate was concentrated in vacuo to give crude product. The crude product was dissolved in MeOH (15 mL) and to it was added diethyl ether (100 mL). The resulting suspension was stirred for 2 hours at room temperature. The solid was filtered to give the title compound (3.62 g, 54%).

後処理

  1. filtrationThe resulting suspension was filtered through a pad of diatomaceous earth (Celite®)
  2. concentrationThe filtrate was concentrated in vacuo
  3. customto give crude product
  4. stirringThe resulting suspension was stirred for 2 hours at room temperature
  5. filtrationThe solid was filtered

出典と根拠

ORDレコード
ord-6f34206cda2b405bb627a938751fc864
出典データセット
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07034152B2

反応ノート

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