HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 3,3,5-Trimethyl-3,5-disila-1-hexene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Silane, (chloromethyl)trimethyl- | HCID 75361 | — |
| Reactant | C4H9ClSi | HCID 57370515 | — |
| Product | 3,3,5-Trimethyl-3,5-disila-1-hexene | HCID 123183472 | 72% |
Reaction Steps
In a procedure analogous to the above paragraph, a Grignard solution was prepared from 68 g (0.55 mol) of chloromethyltrimethylsilane in 150 ml of THF and was then added dropwise at 10° C. to a solution containing chlorodimethylvinylsilane, (available from ABCR GmbH, 7500 Karlsruhe) (2 hours). The mixture was then warmed to room temperature and finally kept at 35° C. for 1 hour, during which a voluminous precipitate formed. Hydrolysis, extraction by shaking with methyl tertbutyl ether, phase separation and working up resulted in 106 g of crude product which on fractionation yielded 68 g (corresponding to 72% of theory) of 3,3,5-trimethyl-3,5-disila-1-hexene (C8H20Si2) at 149°-151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05399290 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-14a53360492d40dcbdd1eb40048a562d |
| Source note | uspto-grants-1995_03 |