Trimethylhydroquinone → HCID 21581684, compound

HRID 2399071Notes

Reaction equation

HRID 2399071 reaction equation
[Cl-].[Al+3].[Cl-].[Cl-].[CH3:5][C:6]1[C:7]([OH:15])=[C:8]([CH3:14])[C:9]([CH3:13])=[C:10]([CH:12]=1)O.[C:16]([O:19][CH2:20][CH2:21][C:22]([OH:26])([CH3:25])[CH:23]=[CH2:24])(=[O:18])[CH3:17]>C(Cl)Cl.[N+](C)([O-])=O>[C:16]([O:19][CH2:20][CH2:21][C:22]1([CH3:25])[CH2:23][CH2:24][C:12]2[C:10](=[C:9]([CH3:13])[C:8]([CH3:14])=[C:7]([OH:15])[C:6]=2[CH3:5])[O:26]1)(=[O:18])[CH3:17]

Participants

6

Procedure

To an ice-cooled mixture of 3.37 g. of aluminum chloride and 40 ml. of methylene chloride was added, dropwise, 3.37 ml. of nitromethane. The resulting solution was stirred 5 minutes, and then 5.114 g. of trimethylhydroquinone was added in one portion. The green mixture was cooled to -20° and a solution of 5.35 g. of 3-hydroxy-3-methyl-4-pentenyl acetate in 20 ml. of methylene chloride was added over 1.0 hour. The mixture was allowed to warm to room temperature, kept there for 2 hours and poured into ice-H2O. The mixture was extracted with methylene chloride and the organic solutions were washed with saturated sodium bicarbonate solution and brine and dried over sodium sulfate. Solvent removal gave crude (±)-2-(2-acetoxyethyl)-6-hydroxy-2,5,7,8-tetramethylchroman as a red oil.

Workup

  1. additionmixture of 3.37 g
  2. temperatureThe green mixture was cooled to -20°
  3. waitkept there for 2 hours
  4. extractionThe mixture was extracted with methylene chloride
  5. washthe organic solutions were washed with saturated sodium bicarbonate solution and brine
  6. dry with materialdried over sodium sulfate
  7. customSolvent removal

Sources & evidence

ORD record
ord-d617c6ac6fb843e78e7b3d2d78880008
Source dataset
uspto-grants-1977_05
Patent number
US04026907

Reaction notes

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