HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorotrimethylsilane → (4-Bromobenzyloxy)trimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 4-Bromobenzyl alcohol | HCID 70119 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (4-Bromobenzyloxy)trimethylsilane | HCID 598201 | — |
Reaction Steps
Trimethylsilyl chloride (1.9 ml, 15 mmol) was added dropwise to a stirred solution of 4-bromobenzyl alcohol (2.0 g, 11 mmol) in toluene (25 ml) and pyridine (2 ml) at 0° C. The stirred mixture was heated to ambient temperature during 3 hours. The reaction mixture was filtered and the organic solution evaporated to yield pure 4-bromobenzyl trimethylsilyl ether. The silyl ether can be further purified by distillation (b.p. 73° C., 0.1 mm Hg). Yield after distillation: 1.49 g (50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06117412 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-c5a8751b84c24c6b91e4c7414af80c74 |
| Source note | uspto-grants-2000_09 |