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Diethyl Ether → 1alpha, 3beta-Bis(tetrahydropyran-2-yloxy)pregna-5,7-diene-20-carbaldehyde

HRID 1708827
ノート
印刷プレビュー

反応式

HRID 1708827 の反応式
[OH:1][C@@H:2]1[C@@:22]2([CH3:23])[C:6](=[CH:7][CH:8]=[C:9]3[C@@H:21]2[CH2:20][CH2:19][C@@:18]2([CH3:24])[C@H:10]3[CH2:11][CH2:12][C@@H:13]2[CH:14]([CH:16]=[O:17])[CH3:15])[CH2:5][C@@H:4]([OH:25])[CH2:3]1.[O:26]1[CH:31]=[CH:30][CH2:29][CH2:28][CH2:27]1.[C:32]1(C)C=[CH:36][C:35](S(O)(=O)=O)=[CH:34][CH:33]=1.CC[O:45]CC>C(Cl)Cl>[O:26]1[CH2:27][CH2:28][CH2:29][CH2:30][CH:31]1[O:1][C@@H:2]1[C@@:22]2([CH3:23])[C:6](=[CH:7][CH:8]=[C:9]3[C@@H:21]2[CH2:20][CH2:19][C@@:18]2([CH3:24])[C@H:10]3[CH2:11][CH2:12][C@@H:13]2[CH:14]([CH:16]=[O:17])[CH3:15])[CH2:5][C@@H:4]([O:25][CH:36]2[CH2:35][CH2:34][CH2:33][CH2:32][O:45]2)[CH2:3]1
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 6101p-Toluenesulfonic acidHCID 80803,4-dihydro-2H-pyranHCID 538927811alpha,3beta-Dihydroxypregna-5,7-diene-20-carbaldehyde

生成物 1

HCID 228438971alpha, 3beta-Bis(tetrahydropyran-2-yloxy)pregna-5,7-diene-20-carbaldehyde

試薬・触媒・溶媒 1

HCID 6344
Dichloromethane
溶媒

実験手順

In 10 ml of methylene chloride was dissolved 0.50 g of 1α,3β-dihydroxypregna-5,7-diene-20-carbaldehyde, followed by addition of 1 ml of 3,4-dihydropyran and 0.05 g of p-toluenesulfonic acid. The mixture was stirred at room temperature for 2 hours. The reaction mixture thus obtained was diluted with ether, washed successively with aqueous sodium hydrogen carbonate solution and aqueous sodium chloride solution, and dried over sodium sulfate, followed by concentration under reduced pressure. Finally the concentrate was purified by column chromatography to give 0.48 g of 1α,3β-bis(tetrahydropyran-2-yloxy)pregna-5,7-diene-20-carbaldehyde showing the following physical properties.

後処理

  1. customThe reaction mixture thus obtained
  2. washwashed successively with aqueous sodium hydrogen carbonate solution and aqueous sodium chloride solution
  3. dry with materialdried over sodium sulfate
  4. concentrationfollowed by concentration under reduced pressure
  5. customFinally the concentrate was purified by column chromatography

出典と根拠

ORDレコード
ord-8c336d8750ea4de89ea8dbec1c9c0374
出典データセット
uspto-grants-1994_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05359055

反応ノート

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