HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (4-(5-Bromo-2-chlorobenzyl)phenoxy)(tert-butyl)dimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 4-((5-Bromo-2-chlorophenyl)methyl)phenol | HCID 57423751 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-(5-Bromo-2-chlorobenzyl)phenoxy)(tert-butyl)dimethylsilane | HCID 59747702 | — |
Reaction Steps
A solution of 13.9 g 4-(5-bromo-2-chloro-benzyl)-phenol in 140 ml dichloromethane is cooled in the ice bath. Then 7.54 g tert-butyldimethylsilylchlorid in 20 ml dichloromethane are added followed by 9.8 ml triethylamine and 0.5 g dimethylaminopyridine. The solution is stirred for 16 h at ambient temperature and then diluted with 100 ml dichloromethane. The organic phase is washed twice with aqueous 1 M hydrochloric acid and once with aqueous sodium hydrogen carbonate solution and then dried over sodium sulphate. After the solvent has been eliminated the residue is filtered through silica gel (cyclohexane/ethyl acetate 100:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07579449B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-2e109b38d6d14e5cbaa02b0ce7d6fbf2 |
| Source note | uspto-grants-2009_08 |