Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | HCID 59808877 | HCID 59808877 | — |
| Reactant | HCID 178419135 | HCID 178419135 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 24808518 | HCID 24808518 | 86% |
Reaction Steps
A mixture of N-(4,6-dimethyl-1-oxo-indan-5-yl)-3,3-dimethyl-butyramide (5 g, 19 mmol), 4-fluoroaniline (5 g, 45 mmol), and decaborane (4.5 g, 36.8 mmol) in 100 ml of anhydrous methanol was stirred for 2 days at room temperature in an high pressure reaction equipment. The reaction mixture was poured into 500 ml of ice-water with strong stirring and the precipitates were filtered and washed with water. The dried solid was crystallized from hexane/ethyl acetate (5:1) to give white crystals (6 g, 86%). 1H-NMR δ (DMSO-d6, 400 MHz): 9.08 (brs, 1H, exchangeable with D2O, NH), 6.98 (s, 1H), 6.92 (t, J=8.8 Hz, 2H), 6.69 (dd, J=4.8 and 8.8 Hz, 2H), 5.76 (d, J=8.0 Hz, 1H, exchangeable with D2O, NH), 4.86 (q, J=8.0 Hz, 1H), 2.86 (ddd, J=4.8, 8.7 and 16.2 Hz, 1H), 2.70 (quint, J=8.1 Hz, 1H), 2.46 (m, 1H), 2.22 (s, 2H), 2.11 (s, 3H), 2.06 (s, 3H), 1.74 (m, 1H), 1.07 (s, 9H). MS: 369 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030518B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-8250b5cc0b2d43979ebe4e908bfb1ff0 |
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| Source note | uspto-grants-2011_10 |
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