HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → tert-Butyldimethyl-[1-(1-propylcyclobutyl)but-3-ynyloxy]silane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl trifluoromethanesulphonate | HCID 123564 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(1-Propylcyclobutyl)but-3-yn-1-ol | HCID 14254776 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-Butyldimethyl-[1-(1-propylcyclobutyl)but-3-ynyloxy]silane | HCID 15475299 | 153.8% |
Reaction Steps
t-Butyldimethylsilyltrifluoromethanesulfonate (1.8 mL, 7.88 mmol) was added to a solution of triethylamine (2.2 mL, 15.8 mmol) and alcohol 4 (650 mg, 3.94 mmol) in CH2Cl2 (5.0 mL) at 0° C. The reaction was stirred for 1 h and then saturated aqueous NaHCO3 was added. The mixture was extracted with CH2Cl2. The organic portion was washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. FCC (silica gel, 100% hexane) gave 1.7 g (100%) of the silyl ether 5 as a clear, colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07314890B2 |
| Source dataset | uspto-grants-2008_01 |
| ORD ID | ord-0331834af2524f36beffdf98d9322b2e |
| Source note | uspto-grants-2008_01 |