HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → (16-Bromohexadecyloxy)-t-butyldimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 16-Bromo-1-hexadecanol | HCID 2757013 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (16-Bromohexadecyloxy)-t-butyldimethylsilane | HCID 86627057 | 81% |
Reaction Steps
16-Bromohexadecan-1-ol (1 g) was dissolved in 20 ml of dichloromethane, and imidazole (317.9 mg) and t-butyldimethylsilyl chloride (701.4 mg) were added to this solution. The reaction mixture was stirred at room temperature for four hours. Saturated ammonium chloride solution was added to the reaction mixture, which was then extracted three times with dichloromethane. The organic layer was washed with saline solution and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure. Purification of the residue by silica gel flash chromatography (heptane:ethyl acetate=7:3) gave (16-bromohexadecyloxy)-t-butyldimethylsilane as a colorless oil at an 81% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893304B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-2280bb53a1af4e60b369dd078465c9a8 |
| Source note | uspto-grants-2011_02 |