HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Tert-butyl(3-ethoxy-2,2-dimethylpropoxy)dimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-{[Tert-butyl(dimethyl)silyl]oxy}-2,2-dimethylpropan-1-ol | HCID 59012138 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl(3-ethoxy-2,2-dimethylpropoxy)dimethylsilane | HCID 23090613 | — |
Reaction Steps
To a solution of 3-{[tert-butyl(dimethyl)silyl]oxy}-2,2-dimethylpropan-1-ol (Registry No. 117932-70-4) (2.18 g, 10 mmol) in THF (30 ml) were added triethylamine (1.67 ml, 12 mmol) and methanesulfonyl chloride (0.85 ml, 11 mmol) under ice cooling. The reaction liquid was stirred at room temperature for 30 minutes, and to the reaction liquid was added an aqueous solution of sodium bicarbonate. The mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give the title compound (2.98 g, quant.) as colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08058280B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-f0c69297ad514922ba44667d65623687 |
| Source note | uspto-grants-2011_11 |