HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tris(1,1-dimethylethyl)phosphine → 2-(2,4,6-Trimethylphenyl)-1H-indene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | 1H-Indene, 2-bromo- | HCID 575586 | — |
| Reactant | HCID 178425415 | HCID 178425415 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 2-(2,4,6-Trimethylphenyl)-1H-indene | HCID 59832553 | — |
Reaction Steps
A mixture of 50.0 ml (20.0 mmol) of 0.4 M mesitylmagnesium bromide in THF, 230 mg (0.40 mmol) of Pd(dba)2, 162 mg (0.80 mmol) of PtBu3, and 3.90 g (20.0 mmol) of 2-bromo-1H-indene was stirred for 48 h at ambient temperature. Then, to the resulting mixture 200 ml of brine was added. The organic layer was separated, and the aqueous layer was extracted with 3×100 ml of ether. The combined organic fractions were dried over K2CO3 and then evaporated to dryness. The product was isolated by flash chromatography on Silica Gel 60 (40-63 um, d 30 mm, 1 300 mm, eluent: hexanes-dichloromethane, 20:1, vol.). Yield 3.19 g (68%) of white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538168B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-5afa249002344910a885f29a22b974dd |
| Source note | uspto-grants-2009_05 |