Scandium(3+);trichloride → HCID 178484171, compound

HRID 1256862Notes

Reaction equation

HRID 1256862 reaction equation
[Cl-].[Sc+3:2].[Cl-].[Cl-].[CH3:5][N:6]([CH:8]([Li])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH3:7]>O1CCCC1>[CH3:5][N:6]([CH:8]([Sc:2]([CH:8]([N:6]([CH3:7])[CH3:5])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH:8]([N:6]([CH3:7])[CH3:5])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[CH3:7]

Participants

4

Procedure

1.0 g (6.6 mmol) of anhydrous scandium chloride and 10 mL of tetrahydrofuran (THF) were placed in a 100 mL glass vessel to prepare a suspension liquid, which was stirred at room temperature for 1 hour. 2.8 g (20 mmol) of the above-obtained dimethylaminobenzyllithium dissolved in 20 mL of THF was added dropwise thereto, followed by stirring for 12 hours. After completing the reaction, THF was removed, and the target compound was extracted with toluene and then purified by recrystallization to provide 2.4 g of tris(dimethylaminobenzyl)scandium (Sc (CH2C6H4N(CH3)2-o)3) as pale yellow crystals (yield: 80%).

Workup

  1. customto prepare a suspension liquid, which
  2. additionwas added dropwise
  3. stirringby stirring for 12 hours
  4. customwas removed
  5. extractionthe target compound was extracted with toluene
  6. custompurified by recrystallization

Sources & evidence

ORD record
ord-70f3059757874f3492a0025b58210e23
Source dataset
uspto-grants-2013_06
Patent number
US08461270B2

Reaction notes

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