No renderable structure data available
C[Si](C)(C)C([Si](C)(C)C)ClChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | [chloro(trimethylsilyl)methyl]-trimethylsilane |
|---|---|
| IUPAC Name | — |
| CAS Number | 5926-35-2 |
| Database ID | 552583 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
[chloro(trimethylsilyl)methyl]-trimethylsilane (CAS 5926-35-2) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
Potential Applications
For professional research and industrial use only
Database ID 552583
Safety Notice
For professional research and industrial use only. Review the supplier safety data sheet before handling.
Synthesis data
10 reactions · 10 references
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-264ab322b52443c68e1811567140e17fConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-f747202c7d134330b523b22f9d3e2191Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Bis(trimethylsilyl)chloromethane (Aldrich) 39 g, 0.2 mole), sodium acrylate (28 g, 0.3 mole), Adogen 464 (Aldrich) (6.96 g), and phenothiazine (0.10 grams) were placed in a round bottom flask equipped with a condenser, mechanical stirrer and a nitrogen inlet. The flask was charged with 100 ml of butyronitrile and heated to reflux while stirring. After 6 hours, the mixture was diluted with 150 ml hexanes and filtered to remove the solids. The solvents were removed under reduced pressure. Fractional distillation of the residue under reduced pressure gave 35.5 grams 975%) of the desired product at 45-58° C. at 0.5 mm pressure. equipped with a condenser, mechanical stirrer and a nitrogen inlet heated to reflux filtered to remove the solids The solvents were removed under reduced pressure Fractional distillation of the residue under reduced pressure
Source ID: ord-0e546afac53e4a3297d14375b599b8eaConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Bis(trimethylsilyl)chloromethane (Aldrich) 39 g, 0.2 mole), sodium acrylate (28 g, 0.3 mole), Adogen 464 (Aldrich) (6.96 g), and phenothiazine (0.10 grams) were placed in a round bottom flask equipped with a condenser, mechanical stirrer and a nitrogen inlet. The flask was charged with 100 ml of butyronitrile and heated to reflux while stirring. After 6 hours, the mixture was diluted with 150 ml hexanes and filtered to remove the solids. The solvents were removed under reduced pressure. Fractional distillation of the residue under reduced pressure gave 35.5 grams 975%) of the desired product at 45-58° C. at 0.5 mm pressure. equipped with a condenser, mechanical stirrer and a nitrogen inlet heated to reflux filtered to remove the solids The solvents were removed under reduced pressure Fractional distillation of the residue under reduced pressure
Source ID: ord-0e546afac53e4a3297d14375b599b8eaConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Bis(trimethylsilyl)chloromethane (Aldrich) (14.68 g, 0.075 mole), sodium methacrylate (8.96 g, 0.0825 mole), Adogen 464 (Aldrich) (1.70 g), and phenothiazine (0.05 grams) were placed in a round bottom flask equipped with a condenser, mechanical stirrer and a nitrogen inlet. The flask was charged with 200 ml acetonitrile and heated to reflux while stirring. After 4 days, the mixture was filtered to remove the solids and the solvent was removed in a rotary evaporator. Fractional distillation under reduced pressure gave 10.90 grams (60% yield) of a clear liquid at 46-48° C. at 0.5 mm pressure. equipped with a condenser, mechanical stirrer and a nitrogen inlet heated to reflux the mixture was filtered to remove the solids the solvent was removed in a rotary evaporator Fractional distillation under reduced pressure
Source ID: ord-de947e5f70ac4014a4c75f782fec3f15Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-264ab322b52443c68e1811567140e17fConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Bis(trimethylsilyl)chloromethane (Aldrich) 39 g, 0.2 mole), sodium acrylate (28 g, 0.3 mole), Adogen 464 (Aldrich) (6.96 g), and phenothiazine (0.10 grams) were placed in a round bottom flask equipped with a condenser, mechanical stirrer and a nitrogen inlet. The flask was charged with 100 ml of butyronitrile and heated to reflux while stirring. After 6 hours, the mixture was diluted with 150 ml hexanes and filtered to remove the solids. The solvents were removed under reduced pressure. Fractional distillation of the residue under reduced pressure gave 35.5 grams 975%) of the desired product at 45-58° C. at 0.5 mm pressure. equipped with a condenser, mechanical stirrer and a nitrogen inlet heated to reflux filtered to remove the solids The solvents were removed under reduced pressure Fractional distillation of the residue under reduced pressure
Source ID: ord-3901f3841ab847a79d34516e6d4156e3Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Bis(trimethylsilyl)chloromethane (Aldrich) (14.68 g, 0.075 mole), sodium methacrylate (8.96 g, 0.0825 mole), Adogen 464 (Aldrich) (1.70 g), and phenothiazine (0.05 grams) were placed in a round bottom flask equipped with a condenser, mechanical stirrer and a nitrogen inlet. The flask was charged with 200 ml acetonitrile and heated to reflux while stirring. After 4 days, the mixture was filtered to remove the solids and the solvent was removed in a rotary evaporator. Fractional distillation under reduced pressure gave 10.90 grams (60% yield) of a clear liquid at 46-48° C. at 0.5 mm pressure. equipped with a condenser, mechanical stirrer and a nitrogen inlet heated to reflux the mixture was filtered to remove the solids the solvent was removed in a rotary evaporator Fractional distillation under reduced pressure
Source ID: ord-e2da1c82b1f34324a34bedf6ba85f15aConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Bis(trimethylsilyl)chloromethane (Aldrich) 39 g, 0.2 mole), sodium acrylate (28 g, 0.3 mole), Adogen 464 (Aldrich) (6.96 g), and phenothiazine (0.10 grams) were placed in a round bottom flask equipped with a condenser, mechanical stirrer and a nitrogen inlet. The flask was charged with 100 ml of butyronitrile and heated to reflux while stirring. After 6 hours, the mixture was diluted with 150 ml hexanes and filtered to remove the solids. The solvents were removed under reduced pressure. Fractional distillation of the residue under reduced pressure gave 35.5 grams 975%) of the desired product at 45-58° C. at 0.5 mm pressure. equipped with a condenser, mechanical stirrer and a nitrogen inlet heated to reflux filtered to remove the solids The solvents were removed under reduced pressure Fractional distillation of the residue under reduced pressure
Source ID: ord-0e546afac53e4a3297d14375b599b8eaConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Bis(trimethylsilyl)chloromethane (Aldrich) (14.68 g, 0.075 mole), sodium methacrylate (8.96 g, 0.0825 mole), Adogen 464 (Aldrich) (1.70 g), and phenothiazine (0.05 grams) were placed in a round bottom flask equipped with a condenser, mechanical stirrer and a nitrogen inlet. The flask was charged with 200 ml acetonitrile and heated to reflux while stirring. After 4 days, the mixture was filtered to remove the solids and the solvent was removed in a rotary evaporator. Fractional distillation under reduced pressure gave 10.90 grams (60% yield) of a clear liquid at 46-48° C. at 0.5 mm pressure. equipped with a condenser, mechanical stirrer and a nitrogen inlet heated to reflux the mixture was filtered to remove the solids the solvent was removed in a rotary evaporator Fractional distillation under reduced pressure
Source ID: ord-de947e5f70ac4014a4c75f782fec3f15PubChem References
These sources are listed in the compound's public database record.
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