Hydrochloric Acid → HCID 15237330, compound

HRID 1655421Notes

Reaction equation

HRID 1655421 reaction equation
O.[OH-].[Li+].[CH3:4][C:5]([C:8]1[CH:9]=[C:10]([S:19][C@@H:20]2[CH2:24][CH2:23][CH2:22][C@H:21]2[S:25][CH2:26][C:27]([O:29]C)=[O:28])[CH:11]=[C:12]([C:15]([CH3:18])([CH3:17])[CH3:16])[C:13]=1[OH:14])([CH3:7])[CH3:6].O.Cl>CO.[Cl-].[Na+].O>[CH3:7][C:5]([C:8]1[CH:9]=[C:10]([S:19][C@@H:20]2[CH2:24][CH2:23][CH2:22][C@H:21]2[S:25][CH2:26][C:27]([OH:29])=[O:28])[CH:11]=[C:12]([C:15]([CH3:16])([CH3:17])[CH3:18])[C:13]=1[OH:14])([CH3:4])[CH3:6]

Participants

7

Procedure

Lithium hydroxide hydrate (1.0 g, 0.025 mole) was added to a solution of the compound of Example 8 (4.13 g, 0.010 mole) in methanol (40 ml). Water (20 ml) Was added over 10 minutes to the reaction mixture. 1.0N hydrochloric acid (25 ml) was added slowly to the reaction mixture followed by water (50 ml) and brine (50 ml). The mixture was extracted twice with 75 ml of diethyl ether. The combined diethyl ether extracts were washed with brine (25 ml), dried over anhydrous magnesium sulfate, filtered and concentrated to an oil by a gentle flow of nitrogen gas. The product was purified by silica gel chromatography. The structure was supported by NMR, infrared spectroscopy and elemental analysis.

Workup

  1. extractionThe mixture was extracted twice with 75 ml of diethyl ether
  2. washThe combined diethyl ether extracts were washed with brine (25 ml)
  3. dry with materialdried over anhydrous magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated to an oil by a gentle flow of nitrogen gas
  6. customThe product was purified by silica gel chromatography

Sources & evidence

ORD record
ord-f5331d02cfbd4d23b0ffa5cf1471a64f
Source dataset
uspto-grants-1993_10
Patent number
US05250567

Reaction notes

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