HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-Bromo-1-(4-trimethylsilanylethynylphenyl)propan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-(4-Trimethylsilanylethynylphenyl)propan-1-one | HCID 67363127 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Bromo-1-(4-trimethylsilanylethynylphenyl)propan-1-one | HCID 87370804 | — |
Reaction Steps
Bromine (8.4 g) is slowly added to 1-(4-trimethylsilanylethynylphenyl)propan-1-one (10.0 g) in 100 ml of tetrahydrofuran at 0° C. and subsequently stirred at room temperature for 2 h. The reaction mixture is diluted with water and extracted with ethyl acetate. The organic layer is washed with brine, dried over sodium sulfate and concentrated under reduced pressure. The remainder is purified by chromatography on silica gel, using a mixture of heptane/ethyl acetate 19:1 as eluent to obtain 2-bromo-1-(4-trimethylsilanylethynylphenyl)propan-1-one as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658644B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-63fffd74425d415bb1f4d9b1bcbe6a17 |
| Source note | uspto-grants-2014_02 |