Barium hydroxide, octahydrate → HCID 25257891, compound

HRID 908121Notes

Reaction equation

HRID 908121 reaction equation
[C:1]12([C:14]([O:16]C)=[O:15])[CH2:9][CH2:8][C:5]([C:10]([O:12][CH3:13])=[O:11])([CH2:6][CH2:7]1)[CH2:4][CH2:3][CH2:2]2.O.O.O.O.O.O.O.O.[OH-].[Ba+2].[OH-]>CO.O>[CH3:13][O:12][C:10]([C:5]12[CH2:6][CH2:7][C:1]([C:14]([OH:16])=[O:15])([CH2:9][CH2:8]1)[CH2:2][CH2:3][CH2:4]2)=[O:11]

Participants

5

Procedure

To a stirred solution of dimethyl bicyclo[3.2.2]nonane-1,5-dicarboxylate (2.02 g, 8.41 mmol), in methanol (20 mL) and water (4 mL) was added barium hydroxide octahydrate (1.33 g, 4.20 mmol). The reaction mixture was stirred vigorously at ambient temperature overnight. The reaction mixture was stirred vigorously at ambient temperature overnight. The reaction mixture was diluted with water (20 mL) and washed with isohexane (2×100 mL), then the aqueous phase was acidified with 2M HCl to pH 2 and extracted into EtOAc (2×100 mL). The organic extracts were combined, dried (MgSO4) and concentrated to leave the title compound (931 mg, 4.11 mmol, 49%) as a clear colourless gum which slowly formed a white solid; 1H NMR (CDCl3) δ 1.72-1.75 (m, 2H), 1.87-1.92 (m, 12H), 3.65 (s, 3H); GC-MS EI m/e M+ 226.

Workup

  1. stirringThe reaction mixture was stirred vigorously at ambient temperature overnight
  2. washwashed with isohexane (2×100 mL)
  3. extractionextracted into EtOAc (2×100 mL)
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-046cb1ea51ef4b43be92e6a2bce866b6
Source dataset
uspto-grants-2011_09
Patent number
US08017603B2

Reaction notes

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