HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 7-(4-Methylbenzyl)benzo[b]thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Benzo[b]thiophen-7-yl-p-tolylmethanol | HCID 68717781 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-(4-Methylbenzyl)benzo[b]thiophene | HCID 67069100 | 89.5% |
Reaction Steps
To a suspension of sodium iodide (2.0 g) in acetonitrile was added chlorotrimethylsilane (1.5 g) at room temperature. After the mixture was stirred at room temperature for 15 minutes, benzo[b]thiophen-7-yl-p-tolylmethanol (0.68 g) was added to the mixture, and the mixture was stirred at room temperature for 15 minutes. The reaction mixture was poured into water, and the mixture was extracted with hexane. The organic layer washed with water and brine and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane) to give the title compound (0.57 g) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732596B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-ba1270ebd64c429686d97f9ef417a6f9 |
| Source note | uspto-grants-2010_06 |