HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → Cyclohexene, 1-((trimethylsilyl)oxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Catalyst | HCID 178482129 | HCID 178482129 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Cyclohexene, 1-((trimethylsilyl)oxy)- | HCID 81161 | 59% |
Reaction Steps
- In another experiment, an enolate is prepared by the reaction of 100 mmol of phenylmanganese N-methyl-N-phenylamide: ##STR11## with 100 mmol of cyclohexanone in 200 ml of THF at 20° C. for 1 hour: ##STR12## 100 mmol of trimethylchlorosilane, ClSiMe3, are added to the resulting solution at 20° C. and the mixture is stirred for 30 minutes to produce the following reaction: ##STR13## 1-Trimethylsilyloxycyclohexene is obtained with a yield of 59%, compared with 77% for procedure A.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05426201 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-4fae0e090ce045e89c782eaa665d0d49 |
| Source note | uspto-grants-1995_06 |