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Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → (1S,5R,6R,7R)-6-[(3S)-3-hydroxy-5-phenyl-1-pentenyl]-7-[(4-phenylbenzoyl)oxy]-2-oxabicyclo[3.3.0]octane-3-one

HRID 584878
Notes
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Reaction equation

HRID 584878 reaction equation
C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1.[C:18]1([C:24]2[CH:59]=[CH:58][C:27]([C:28]([O:30][C@@H:31]3[CH2:39][C@@H:34]4[O:35][C:36](=[O:38])[CH2:37][C@@H:33]4[C@H:32]3/[CH:40]=[CH:41]/[C@@H:42]([O:51]C3CCCCO3)[CH2:43][CH2:44][C:45]3[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=3)=[O:29])=[CH:26][CH:25]=2)[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>CO>[OH:51][C@@H:42]([CH2:43][CH2:44][C:45]1[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=1)/[CH:41]=[CH:40]/[C@@H:32]1[C@@H:33]2[C@@H:34]([O:35][C:36](=[O:38])[CH2:37]2)[CH2:39][C@H:31]1[O:30][C:28](=[O:29])[C:27]1[CH:58]=[CH:59][C:24]([C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)=[CH:25][CH:26]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 10188059(3aR,4R,5R,6aS)-Hexahydro-5-(p-phenylbenzoyloxy)-4-[(3S)-5-phenyl-3-[(tetrahydro-2H-pyran-2-yl)oxy]-1E-pentenyl]-2H-cyclopenta[b]furan-2-one

Product 1

HCID 10322987(1S,5R,6R,7R)-6-[(3S)-3-hydroxy-5-phenyl-1-pentenyl]-7-[(4-phenylbenzoyl)oxy]-2-oxabicyclo[3.3.0]octane-3-oneYield 81%

Reagents, catalysts & solvents 1

HCID 887
Methanol
Solvent

Conditions

Temperature
45 °C

Procedure

Pyridinium p-toluenesulfonate (50 mg) was added to a stirred solution of the compound [7a] (1.00 g) in methanol (50 mL) at room temperature. The mixture was stirred at 40-50° C. for 3-4 hours (TLC monitoring) and evaporated under reduced pressure. The residue was diluted with dichloromethane (75 mL). The solution was washed with saturated aqueous solution of sodium bicarbonate (25 mL) and brine(25 mL), dried over sodium sulfate, filtered and evaporated to give 0.69 g (81.0%) of oily residue. The residue was crystallized from a mixture of ethyl acetate and isopropyl ether to give compound [5a] as white crystals with mp 126-128° C. 1H NMR (CDCl3) is in agreement with the structure.

Workup

  1. customevaporated under reduced pressure
  2. additionThe residue was diluted with dichloromethane (75 mL)
  3. washThe solution was washed with saturated aqueous solution of sodium bicarbonate (25 mL) and brine(25 mL)
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. customevaporated

Sources & evidence

ORD record
ord-90f6ca91168b45578b6d383026930c0b
Source dataset
uspto-grants-2005_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06927300B2

Reaction notes

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