HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Methyldichlorosilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | HCID 88011121 | HCID 88011121 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyldichlorosilane | HCID 6376 | — |
| Product | Trichloromethylsilane | HCID 6399 | — |
Reaction Steps
As control experiments, the ammonolysis of CH3SiCl3 alone was studied. Ammonolysis of this precursor in Et2O gave a 46% yield of soluble solid product, molecular weight 702 g/mol. ceramic yield (by TGA to 950° C.) 56%. A similar CH3SiCl3 /NH3 reaction in THF gave soluble solid product in 82% yield, molecular weight 672 g/mol, ceramic yield (by TGA) 69%. By proton NMR (CH3Si/NH integration), the Et2O product may be formulated as [CH3Si(NH)1.3 ]x, the THF product as [CH3Si(NH)1.6 ]x. (This is only a rough approximation because integration of the broad NH signals is rather inaccurate). The results of the coammonolyses of CH3SiHCl2 and CH3SiCl3 are given in Tables 4 and 5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04720532 |
| Source dataset | uspto-grants-1988_01 |
| ORD ID | ord-db07fe4c714247efa1684627ab53a73e |
| Source note | uspto-grants-1988_01 |