Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 1H-inden-1-one | HCID 11815384 | — |
| Reactant | Phenyl-d5-boronic acid | HCID 16213772 | — |
| Catalyst | Bis(norbornadiene)rhodium(I) tetrafluoroborate | HCID 10915722 | — |
| Solvent | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Product | 1-Indanone | HCID 6735 | — |
Reaction Steps
To a solution of compound A (57 g) in tetrahydrofuran (600 mL) was added triethylamine (30 mL) dropwise over 30 min. The reaction mixture was kept at room temperature for 3 hours. The precipitated solid was filtered and the filtrate was concentrated in vacuo. The residue was reprecipitated from diethyl ether to afford compound B (31 g) as a yellow solid. To a solution of compound phenyl-d5-boronic acid (25 g) in 1,4-dioxane/water (900 mL/90 mL) was added [Rh(ndb)2]BF4 (1.3 g), racemic BINAP (2.1 g) and triethylamine (14 mL), then the reaction mixture was kept at room temperature for 2 hours under N2. Then compound indenone (19 g) was added, and the resulting mixture was heated to 100° C. for 3 hours. The precipitated solid was filtered off. The filtrate was concentrated in vacuo. The residue was purified by chromatography to afford indanone C (10 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09012453B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-c5a461124c49411c941ee37db87611e1 |
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| Source note | uspto-grants-2015_04 |
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