HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → {[1-(4-Fluorophenoxy)but-3-yn-2-yl]oxy}(trimethyl)silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 1-(4-Fluorophenoxy)but-3-yn-2-ol | HCID 12786216 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | {[1-(4-Fluorophenoxy)but-3-yn-2-yl]oxy}(trimethyl)silane | HCID 12786217 | 91% |
Reaction Steps
To a 0° C solution of 10 g (55 mmoles) of 3-hydroxy-4-p-fluorophenoxy-1-butyne (Example 157) in 75 ml of dry dimethylformamidee and 88 g (130 mmoles) of imidazole is added dropwise, with stirring, 7.5 g (68 mmoles) of chlorotrimethylsilane. The mixture, while under an argon atmosphere, is stirred at room temperature for 18 hours, and then poured into 150 ml of hexane and 100 ml of ice-water. Thhe organic phase is separated, washed with 50 ml of a brine solution, dried with magnesium sulfate, and evaporated under vacuum. This crude product is distilled under vacuum at 0.1 mm (bp 73°-75° C), to give 12.2 g (91%) of the subject compound as a colorless oily liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04085272 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-59aa7426e6ac48f89a234eb1d20fc1c7 |
| Source note | uspto-grants-1978_04 |