Dimethyl Sulfate → 3-(3,5,5,8,8-Pentamethyl-5,6,7,8-tetrahydro-2-naphthyl)-4,6-dimethoxybenzaldehyde

HRID 488822Notes

Reaction equation

HRID 488822 reaction equation
[CH3:1][C:2]1[C:3]([C:16]2[CH:17]=[C:18]([C:21]([OH:26])=[CH:22][C:23]=2[O:24][CH3:25])[CH:19]=[O:20])=[CH:4][C:5]2[C:6]([CH3:15])([CH3:14])[CH2:7][CH2:8][C:9]([CH3:13])([CH3:12])[C:10]=2[CH:11]=1.[CH3:27]OS(OC)(=O)=O.C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[CH3:1][C:2]1[C:3]([C:16]2[CH:17]=[C:18]([C:21]([O:26][CH3:27])=[CH:22][C:23]=2[O:24][CH3:25])[CH:19]=[O:20])=[CH:4][C:5]2[C:6]([CH3:15])([CH3:14])[CH2:7][CH2:8][C:9]([CH3:12])([CH3:13])[C:10]=2[CH:11]=1

Participants

5

Procedure

To a solution of 3-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthyl)-4-methoxy-6-hydroxybenzaldehyde (1.04 g, 2.95 mmol) in acetone (20 mL) was added dimethylsulfate (0.37 mL, 3.84 mmol) and potassium carbonate (490 mg, 3.55 mmol). The reaction mixture was stirred at room temperature for 15 hours and extracted with ethyl acetate (2×50 mL). The organic extracts were successively washed with water (100 mL) and a saturated aqueous solution of NaCl (100 mL), dried over MgSO4 and filtered. Removal of the solvent under reduced pressure gave 3-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthyl)-4,6-dimethoxybenzaldehyde (1.05 g, 97%).

Workup

  1. extractionextracted with ethyl acetate (2×50 mL)
  2. washThe organic extracts were successively washed with water (100 mL)
  3. dry with materiala saturated aqueous solution of NaCl (100 mL), dried over MgSO4
  4. filtrationfiltered
  5. customRemoval of the solvent under reduced pressure

Sources & evidence

ORD record
ord-16a3deb156eb461d992c7175b9c39f36
Source dataset
uspto-grants-2005_12
Patent number
US06974826B2

Reaction notes

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