Acetone → HCID 23287942, compound

HRID 1954126Notes

Reaction equation

HRID 1954126 reaction equation
[CH2:1]([N:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]CC=C.C[N+]1([O-])CC[O:22]CC1.[CH3:26][C:27]([CH3:29])=[O:28]>O>[OH:22][CH2:26][CH:27]([OH:28])[CH2:29][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH2:1][N:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1

Participants

5

Procedure

A solution of N-(10-undecenyl)piperidine (3.1 g, 13 mmol), 4-methylmorpholine-N-oxide (1.84 g, 15.7 mmol) and potassium osmate dihydrate (13 mg) in acetone (64 mL) and water (16 mL) were stirred for 6 hours. The reaction was quenched by the addition of 25 mL of a saturated solution of sodium sulphite and stirred for 15 minutes. The reaction mixture was then extracted with ethyl acetate (4×100 mL), the combined organic extract was dried over anhydrous magnesium sulphate and concentrated under reduced pressure. The crude product obtained was further purified by flash chromatography over silica gel using 10% methanol/ethyl acetate eluant to yield 2.5 g (83.4% yield) N-(11,10-dihydroxyundecyl)piperidine (inventive compound no. 1622).

Workup

  1. customThe reaction was quenched by the addition of 25 mL of a saturated solution of sodium sulphite
  2. extractionThe reaction mixture was then extracted with ethyl acetate (4×100 mL)
  3. extractionthe combined organic extract
  4. dry with materialwas dried over anhydrous magnesium sulphate
  5. concentrationconcentrated under reduced pressure
  6. customThe crude product obtained
  7. customwas further purified by flash chromatography over silica gel using 10% methanol/ethyl acetate eluant

Sources & evidence

ORD record
ord-4527f81327a846d88929d2e1d357ee01
Source dataset
uspto-grants-2000_09
Patent number
US06121270

Reaction notes

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