HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → (3-Fluoro-4-nitrobenzyloxy)triisopropylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Triisopropylsilyl trifluoromethanesulfonate | HCID 2724529 | — |
| Reactant | 3-Fluoro-4-nitrobenzyl alcohol | HCID 2774658 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3-Fluoro-4-nitrobenzyloxy)triisopropylsilane | HCID 60195384 | 99% |
Reaction Steps
To a 3-L round-bottomed flask was added (3-fluoro-4-nitrophenyl)methanol (4.7 g, 27.5 mmol) and DCM (47 mL). To the mixture was added triisopropylsilyl trifluoromethanesulfonate (9.26 g, 30.2 mmol) and 2,6-dimethylpyridine (3.53 g, 33.0 mmol). The resulting mixture was stirred for 3 hours at RT, and washed with NH4Cl (5-250 mL) and H2O (5-250 mL). The organic layer was collected and dried over sodium sulfate and concentrated to afford (3-fluoro-4-nitrobenzyloxy)triisopropylsilane (8.9 g, 99% yield) as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115127B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-78eca634cba14ca0a10bcf6f69fde987 |
| Source note | uspto-grants-2015_08 |