Chlorotrimethylsilane → Stannane, chlorotricyclohexyl-

HRID 501918

Reaction equation

HRID 501918 reaction equation
C[Si]([Cl:5])(C)C.[OH-].[CH:7]1([Sn+:13]([CH:20]2[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21]2)[CH:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1>>[CH:20]1([Sn:13]([Cl:5])([CH:7]2[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12]2)[CH:14]2[CH2:19][CH2:18][CH2:17][CH2:16][CH2:15]2)[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25]1

Participants

3

Reactant 2

HCID 6397ChlorotrimethylsilaneHCID 9864905Cyhexatin

Product 1

HCID 76539Stannane, chlorotricyclohexyl-

Procedure

In a 500 mL three-necked flask, trimethylsilyl chloride (170 g, 109 mmol) was added to tricyclohexyltin hydroxide (80 g, 133 mmol) and heated at reflux during 18 hours. After distillation of trimethylsilyl chloride in excess and hexamethyldisiloxane under reduced pressure, the crude product was recrystallized in petroleum ether. White needles were obtained (39.82 g, 79.6 mmol).

Workup

  1. temperatureheated
  2. temperatureat reflux during 18 hours
  3. distillationAfter distillation of trimethylsilyl chloride in excess and hexamethyldisiloxane under reduced pressure
  4. customthe crude product was recrystallized in petroleum ether
  5. customWhite needles were obtained (39.82 g, 79.6 mmol)

Sources & evidence

ORD record
ord-93315c5e7b7e4903937b9806282aec0b
Source dataset
uspto-grants-2010_08
Patent number
US07772417B2

Linked notes

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