HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Thiosulfate → 2-bromo-1-(3-{[tert-butyl(dimethyl)silyl]oxy}phenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 1-(3-{[tert-Butyl(dimethyl)silyl]oxy}phenyl)ethan-1-one | HCID 14361489 | — |
| Reactant | Phenyltrimethylammonium bromide dibromide | HCID 17977687 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-bromo-1-(3-{[tert-butyl(dimethyl)silyl]oxy}phenyl)ethanone | HCID 11645608 | — |
Reaction Steps
To a solution (40 mL) of the compound (9.4 g, 37 mmol) obtained in Example 38a in diethyl ether was added phenyltrimethylammonium tribromide (14 g, 37 mmol), and the mixture was stirred at room temperature for 5 hr. After confirmation of the termination of the reaction by TLC, aqueous sodium thiosulfate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give a crude title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461348B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-54a7c394510e48d29995ed5f9065b186 |
| Source note | uspto-grants-2013_06 |