HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → 1,2-Difluoro-3-trimethylsilylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 1,2-Difluorobenzene | HCID 9706 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,2-Difluoro-3-trimethylsilylbenzene | HCID 10899371 | — |
Reaction Steps
625 ml (1 mol) of 1.6 M BuLi are added dropwise at −78° C. to a solution of 114 g (1 mol) of 1,2-difluorobenzene in 1 l of dry tetrahydrofuran. After 1 hour, 140 ml (120 g, 1.1 mol) of trimethylsilyl chloride are slowly added dropwise at −78° C. The mixture is allowed to warm to room temperature overnight, and then 200 ml of methyl tert-butyl ether and 200 ml of water are added. The organic phase is washed with water (2×100 ml) and sat. NaCl (1×100 ml) and dried using magnesium sulfate, and the solvent is removed under reduced pressure. 170 g (91%) of 5 distil over from the residue at from 100 to 102° C./70 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07183447B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-5b4a85235cc44b289503edb92ef623ce |
| Source note | uspto-grants-2007_02 |