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

HRID 1708827
Notes
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Reaction equation

HRID 1708827 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 3283Diethyl EtherHCID 6101p-Toluenesulfonic acidHCID 80803,4-dihydro-2H-pyranHCID 538927811alpha,3beta-Dihydroxypregna-5,7-diene-20-carbaldehyde

Product 1

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

Reagents, catalysts & solvents 1

HCID 6344
Dichloromethane
Solvent

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-8c336d8750ea4de89ea8dbec1c9c0374
Source dataset
uspto-grants-1994_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05359055

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes