1-Tetralone → HCID 53980641, compound

HRID 1448121Notes

Reaction equation

HRID 1448121 reaction equation
[CH2:1]1[CH2:11][C:9](=[O:10])[C:8]2[C:3](=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH2:2]1.[CH3:12][N:13]([CH3:26])[CH2:14][CH2:15][CH2:16][O:17][C:18]1[CH:25]=[CH:24][C:21]([CH:22]=O)=[CH:20][CH:19]=1.[OH-].[K+]>C(O)C>[CH3:26][N:13]([CH3:12])[CH2:14][CH2:15][CH2:16][O:17][C:18]1[CH:19]=[CH:20][C:21]([CH:22]=[C:11]2[CH2:1][CH2:2][C:3]3[C:8](=[CH:7][CH:6]=[CH:5][CH:4]=3)[C:9]2=[O:10])=[CH:24][CH:25]=1

Participants

5

Reactant 3

HCID 107241-TetraloneHCID 14797Potassium HydroxideHCID 5469324-[3-(Dimethylamino)propoxy]benzaldehyde

Product 1

HCID 53980641HCID 53980641, compoundYield 75.9%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent2×

Procedure

A stirred solution of 50 g of α-tetralone and 70 g of 4-(3-dimethylaminopropoxy)benzaldehyde in 275 ml of ethanol is cooled to -20° C. and treated with 2.0 g of potassium hydroxide dissolved in 50 ml of ethanol. The cooling bath is removed and after standing for about 16 hours at room temperature the reaction mixture (some product has separated) is added to 1.2 liters of cold water. The material is extracted with 3:1 ether-dichloromethane (five 300 ml portions), the combined extracts are dried over magnesium sulfate, and the solvents are removed on a rotary evaporator to give a semi-solid residue. Crystallization of the residue from 300 ml of diisopropyl ether yields 86 g of product; melting point 86°-88° C.

Workup

  1. customThe cooling bath is removed
  2. customthe reaction mixture (some product has separated)
  3. additionis added to 1.2 liters of cold water
  4. extractionThe material is extracted with 3:1 ether-dichloromethane (five 300 ml portions)
  5. dry with materialthe combined extracts are dried over magnesium sulfate
  6. customthe solvents are removed on a rotary evaporator
  7. customto give a semi-solid residue
  8. customCrystallization of the residue from 300 ml of diisopropyl ether

Sources & evidence

ORD record
ord-3347a18d50f34ca38fdbf8ce163f1c24
Source dataset
uspto-grants-1979_12
Patent number
US04179558

Reaction notes

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