HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-(4-Bromophenethyl)-1-methoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Bromophenethyl bromide | HCID 11010825 | — |
| Reactant | HCID 178491912 | HCID 178491912 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | 4-(4-Bromophenethyl)-1-methoxybenzene | HCID 13548081 | — |
Reaction Steps
4-Bromophenethyl bromide (261.4 mg, 1.0 mmol) and a THF solution (1.42 mL, 1.06 M, 1.5 mmol) of 4-methoxyphenylmagnesium bromide were used as starting materials, and reacted as in Entry 1. Conditions: The THF solution of 4-methoxyphenylmagnesium bromide was added dropwise at 40° C. over 3 hours. After thin-layer chromatography (hexane/ethyl acetate=92/8), the title compound was obtained as a colorless liquid (0.226 g, yield 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637710B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-20fcc1df6c73470c853001b20beeb23b |
| Source note | uspto-grants-2014_01 |