HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Chloride → Tert-butyl-hexadecane-15-ynyloxy-dimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Chloride | HCID 4873 | — |
| Reactant | 14-Bromo-1-(t-butyldimethylsiloxy)tetradecane | HCID 11675874 | — |
| Reactant | HCID 178464060 | HCID 178464060 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Tert-butyl-hexadecane-15-ynyloxy-dimethylsilane | HCID 23073442 | 81.1% |
Reaction Steps
The solution of (14-bromo-tetradecyloxy)-tert-butyl-dimethylsilane (8.9 g, 21.4 mmol, 1 eq) in DMSO (10 mL) was added dropwise to the solution of N,N-diethylethane-1,2-diamine lithium acetylide (3.1 g, 33.2 mmol, 1.5 eq) in DMSO (15 mL) at 0° C. This solution was stirred at room temperature for 6 hours, poured into saturated aqueous solution of potassium chloride (100 mL), and extracted three times with hexane (100 mL). The extract was washed with aqueous solution of sodium chloride, dried over magnesium sulfate, and concentrated. The resulting concentrate was subjected to silica gel flush column chromatography (eluate: hexane-CH2Cl2=80-20) to obtain the colorless liquid of the title compound (6.12 g, yield 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07307098B2 |
| Source dataset | uspto-grants-2007_12 |
| ORD ID | ord-c9bbc06960394a3cad966d33a13ca9ea |
| Source note | uspto-grants-2007_12 |