Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Thiopheneboronic acid | HCID 2733960 | — |
| Reactant | 7-Bromo-2-methyl-2,3-dihydro-1H-inden-1-one | HCID 15869783 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Tris(o-tolylphenyl)phosphine | HCID 22172997 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-Methyl-7-(2-thienyl)-1-indanone | HCID 22173119 | 75.3% |
Reaction Steps
Using a method similar to Example 15a), 11.25 g (0.05 mol) of (2), 13.4 g (0.055 mol) of thiophenylboronic acid and 11.7 g (0.11 mol) of sodium carbonate were placed in 190 ml of dimethoxyethane and 60 ml of water in the reaction vessel, the mixture was degassed a number of times and saturated with argon. 225 mg (1 mmol) of palladium acetate and 0.609 g (2 mmol) of tris(o-tolylphenyl)phosphine were added and the reaction mixture was stirred for 2 hours at 80° C. After addition of 150 ml of water, the mixture was extracted 4 times with 100 ml each time of diethyl ether, the ether phase was washed twice with 50 ml each time of water and dried over magnesium sulfate. Removal of the solvent gave 8.6 g of (22) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06492539B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-60a25d30274e480db4cecc021b6d2ce6 |
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| Source note | uspto-grants-2002_12 |
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