HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → 3-(4-Methoxycarbonylphenyl)-1-trimethylsilyloxy-1-propene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 4-(3-oxopropyl)benzoate | HCID 10104031 | — |
| Solvent | Bicarbonate Ion | HCID 769 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4-Methoxycarbonylphenyl)-1-trimethylsilyloxy-1-propene | HCID 54382847 | — |
Reaction Steps
9.61 g (50 mmol) 3-(4-Methoxycarbonylphenyl)propanal are dissolved, together with 8.3 ml (68 mmol) of trimethylchlorosilane and 18.1 ml (0.13 mol) of triethylamine, in 15 ml of absolute dimethyl formamide and the solution is heated under reflux for 2 hours under nitrogen. After cooling, the reaction mixture is diluted with a saturated bicarbonate solution and extracted with petroleum ether. The organic phase is washed 3 times with a saturated bicarbonate solution, dried with sodium sulphate and concentrated by evaporation. The residue is distilled under a high vacuum (distillation apparatus silylated). 11.06 g of a pale yellow, oily product are thus obtained in the form of a mixture of the cis- and trans-isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05041638 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-b09fc1839cc34da59f989f119cdc6dc8 |
| Source note | uspto-grants-1991_08 |