2-Methyl-2-butene → HCID 86664271, compound

HRID 2387738Notes

Reaction equation

HRID 2387738 reaction equation
CC(=CC)C.P([O-])(O)(O)=O.[Na+].[Cl:12][C:13]1[N:18]=[C:17]([CH3:19])[C:16]([O:20][CH2:21][C@@:22]2([C:27]3[CH:32]=[CH:31][CH:30]=[C:29]([F:33])[CH:28]=3)[CH2:24][C@H:23]2[CH:25]=[O:26])=[CH:15][N:14]=1.Cl([O-])=[O:35].[Na+]>O.CC(C)=O.O>[Cl:12][C:13]1[N:18]=[C:17]([CH3:19])[C:16]([O:20][CH2:21][C@@:22]2([C:27]3[CH:32]=[CH:31][CH:30]=[C:29]([F:33])[CH:28]=3)[CH2:24][C@H:23]2[C:25]([OH:35])=[O:26])=[CH:15][N:14]=1

Participants

7

Procedure

2-methyl-2-butene (11.7 ml) and sodium dihydrogen phosphate (3.98 g) were added to an acetone-water (80 ml-20 ml) solution of the compound 323-2 (7.1 g). The reaction solution was cooled on ice. Sodium chlorite (4 g) was added to the reaction solution, and the obtained mixture was stirred at room temperature for 18 hours. Water was added to the reaction solution, and the mixture was extracted with ethyl acetate. The obtained organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-heptane:ethyl acetate=9:1 to 3:7), so as to obtain the title compound (5.77 g).

Workup

  1. temperatureThe reaction solution was cooled on ice
  2. extractionthe mixture was extracted with ethyl acetate
  3. dry with materialThe obtained organic layer was dried over magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe obtained residue was purified by silica gel column chromatography (n-heptane:ethyl acetate=9:1 to 3:7)

Sources & evidence

ORD record
ord-068a277008d743218e4b32369ab7db6c
Source dataset
uspto-grants-2012_09
Patent number
US08268848B2

Reaction notes

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