tert-Butyl methyl ether → HCID 42598638, compound

HRID 2428288Notes

Reaction equation

HRID 2428288 reaction equation
[OH:1][C:2]1[C:3]([CH3:23])=[C:4]2[C:9](=[C:10]([CH3:13])[C:11]=1[CH3:12])[O:8][C:7]([C:15]([N:17]1[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1)=[O:16])([CH3:14])[CH2:6][CH2:5]2.CC([O:28]C)(C)C>O>[OH:28][C:7]([CH3:14])([C:15](=[O:16])[N:17]1[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]1)[CH2:6][CH2:5][C:4]1[C:9](=[O:8])[C:10]([CH3:13])=[C:11]([CH3:12])[C:2](=[O:1])[C:3]=1[CH3:23]

Participants

4

Procedure

A solution of 319 mg of (6-hydroxy-2,5,7,8-tetramethylchroman-2-yl)(piperidin-1-yl)methanone (1.02 mmol) in 5 mL MTBE which was treated with 1.077 g FeCl3.6H2O in 6 mL H2O. The reaction mixture rapidly turned black which faded to a yellow color over the course of the reaction. An additional 2 mL MTBE was added and stirred vigorously for 3 h at room temp. The reaction was quenched with 10 mL H2O and 10 mL MTBE, the layers separated and the organics washed with H2O until colorless. The combined aqueous phases were extracted 2×10 mL MTBE and the combined organics washed with saturated NaCl and dried over Na2SO4. Flash chromatography yielded 335 mg of 2-(3-hydroxy-3-methyl-4-oxo-4-(piperidin-1-yl)butyl)-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione as a dark yellow oil.

Workup

  1. customThe reaction mixture rapidly turned black which faded to a yellow color over the course of the reaction
  2. customThe reaction was quenched with 10 mL H2O and 10 mL MTBE
  3. customthe layers separated
  4. washthe organics washed with H2O until colorless
  5. extractionThe combined aqueous phases were extracted 2×10 mL MTBE
  6. washthe combined organics washed with saturated NaCl
  7. dry with materialdried over Na2SO4

Sources & evidence

ORD record
ord-efddf5d225dc462db60c67a0306a9460
Source dataset
uspto-grants-2011_06
Patent number
US07968746B2

Reaction notes

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