Sodium Hydroxide → HCID 86747631, compound

HRID 1449645Notes

Reaction equation

HRID 1449645 reaction equation
C([O:4][C@H:5]1[CH2:18][C@@H:17]([O:19]C(=O)C)[C@H:16](/[CH:23]=[CH:24]/[CH:25]=[CH:26]/[CH2:27][CH2:28][CH2:29][CH3:30])[C@H:6]1[CH2:7]/[CH:8]=[CH:9]\[CH2:10][CH2:11][CH2:12][C:13]([OH:15])=[O:14])(=O)C.[OH-].[Na+]>CO>[OH:4][C@H:5]1[CH2:18][C@@H:17]([OH:19])[C@H:16](/[CH:23]=[CH:24]/[CH:25]=[CH:26]/[CH2:27][CH2:28][CH2:29][CH3:30])[C@H:6]1[CH2:7]/[CH:8]=[CH:9]\[CH2:10][CH2:11][CH2:12][C:13]([OH:15])=[O:14]

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 86747632HCID 86747632, compound

Product 1

HCID 86747631HCID 86747631, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

The compound 121 obtained above (3.90 g, 9.27 mmole) was dissolved in methanol (40 ml), and 10% aqueous sodium hydroxide was added to the solution, and the mixture was stirred at room temperature for one hour. Then, the mixture was treated following the procedure similar to that of Example 44 to yield a residue (2.84 g). The residue was purified with Lobar column (ethyl acetate: n-hexane: acetic acid=50:50:1), to yield the title compound 122 (2.67 g, 84%).

Workup

  1. additionThen, the mixture was treated

Sources & evidence

ORD record
ord-767622b4ebb64c71bd212d863db7f4f0
Source dataset
uspto-grants-1997_02
Patent number
US05599837

Reaction notes

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