HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Chloromethyldimethyl-2-phenylethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Silane, chloro(chloromethyl)dimethyl- | HCID 74393 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178419670 | HCID 178419670 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Chloromethyldimethyl-2-phenylethylsilane | HCID 22399658 | 48.5% |
Reaction Steps
To a solution of 2-phenylethylmagnesium bromide, prepared from 2-phenylethyl bromide (9.25 g, 50 mmol) and magnesium (1.34 g, 55 mmol) in tetrahydrofuran (50 ml), is added chlorochlormethyldimethylsilane (6.43 g, 45 mmol) in tetrahydrofuran (25 ml). The mixture is refluxed for 18 hours, cooled to 0° C. and hydrolyzed with 3N HCl (50 ml). The mixture is then poured in water (50 ml) and diethyl ether (50 ml), the organic layer is washed with water, brine, dried over MgSO4 and the solvents removed in vacuo. Fractional distillation affords the title compound (5.15 g, 48.5% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05529988 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-6a12f37e08094ca1adf45eec0b590c59 |
| Source note | uspto-grants-1996_06 |