HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → [(1-Ethyl-1-propen-1-yl)oxy]trimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Ethyl ketone | HCID 7288 | — |
| Product | [(1-Ethyl-1-propen-1-yl)oxy]trimethylsilane | HCID 53689637 | — |
Reaction Steps
From reaction between diethylketone and trimethylchlorosilane to form 3-trimethylsilyloxy-2-pentene(1.2.4.17). This product was reacted with 1-fluoropyridinium triflate(1.2.4.5) to obtain 2-fluoro-3-pentanone(1.2.4.9). After bromination with pyridinium bromide followed by reduction using diborane 2-fluoro-4-bromopentane-3-ol(1.2.4.18) was obtained. Reaction of this product with sodium methylate yielded the title compound (1.2.4.16). This compound was made also by reacting 2-(1-bromoethyl)-3-methyl oxirane(1.2.4.13) with HF/Py (70%) followed by treatment of the resulting 2-bromo-4-fluoropentan-3-ol(1.2.4.18) with K2CO3/MeOH.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06583182B1 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-3ff2deed151246f1b54dbd26f95b6898 |
| Source note | uspto-grants-2003_06 |