HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroiodomethane → 1-Bromo-4-cyclopropoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroiodomethane | HCID 11644 | — |
| Reactant | 1-Bromo-4-(ethenyloxy)benzene | HCID 11401372 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 1-Bromo-4-cyclopropoxybenzene | HCID 50998694 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
39.0 g (176 mmol) 1-Bromo-4-vinyloxybenzene and 32.4 mL (441 mmol) chloroiodomethane are added to 500 mL dichloroethane and cooled to 0° C. During 1 h 200 mL (200 mmol) diethylzinc solution (c=1 mol/l in hexane) are added and stirring is continued for 2 h at 0° C. The reaction is quenched by the addition of 200 mL of a sat. aq. NH4Cl solution and extracted with TBME (2×). The organic phases are combined, washed with brine, dried over MgSO4 and the solvent is removed in vacuo. The crude product is purified by column chromatography (silica gel, PE).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08759528B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-0821604af10a42ccbd7d699a7898a68e |
| Source note | uspto-grants-2014_06 |