HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3,5,6-Tetrafluorophenol → HCID 18332211, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3,5,6-Tetrafluorophenol | HCID 69858 | — |
| Reactant | Silane, (chloromethyl)triethoxy- | HCID 84858 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18332211 | HCID 18332211 | — |
Reaction Steps
3.32 g (20 mmol) of 2,3,5,6-tetrafluorophenol are dissolved in 50 ml of toluene, and 8 ml of n-butyllithium (2.5 M in hexane) are added at 0° C. After warming to room temperature, the solution is stirred for a further 2 hours. Then 4.3 g of (chloromethyl)triethoxysilane (20 mmol) are added dropwise and the reaction mixture is boiled under reflux for 6 hours. The resulting suspension is filtered and the solvent is stripped off in vacuo. The pale yellow liquid which remains is subjected to fractional distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329313B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-ebfb8748caf74c449315714feedfccce |
| Source note | uspto-grants-2001_12 |