Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Bromoanisole | HCID 11358 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Reactant | HCID 178422466 | HCID 178422466 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178489288 | HCID 178489288 | 26% |
Reaction Steps
To a solution of 2.25 g (5.0 mmol) of 34 in 20 mL of THF, 4.0 mL (10.0 mmol) of 2.5 M nBuLi in hexanes was added at −80° C. This mixture was stirred for 1 hr, then cooled to −100° C. and 10.8 mL (10.8 mmol) of 1.0 M ZnCl2 in THF was added. The resulting mixture was slowly warmed to ambient temperature, stirred for 30 min, and then 2.82 g (15.0 mmol) of 2-bromoanisole and 0.14 g (0.25 mmol) of Pd(PtBu3)2 was added. This mixture was refluxed for 8 hr, then 5 mL of water was added. The resulting mixture was passed through a short layer of silica gel 60. The silica gel layer was additionally washed with 30 mL of dichloromethane. The combined organic elute was evaporated to dryness. The product was isolated by flash chromatography on silica gel 60 (40-63 um, eluent: from hexanes to hexanes-diethyl ether, 20:1, vol.) to give 0.55 g (26%) of a yellowish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08541521B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-ba38f7d4036a42b983404df945cc5402 |
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| Source note | uspto-grants-2013_09 |
|---|