Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butanal | HCID 261 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Bromo-5-iodobenzonitrile | HCID 45040712 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67980648 | HCID 67980648 | 80.6% |
Reaction Steps
A round bottom flask was charged with the 2-bromo-5-iodobenzonitrile (2.00 g, 6.49 mmol) and THF (9 mL). Solution cooled down to −8° C. (ice/brine bath). Turbo Grignard 1.3M in THF (5.50 mL, 7.14 mmol) is then added in one portion and the reaction stirred for 15 minutes at −8° C. Butyraldehyde (0.698 μL, 7.79 mmol) is then charged in another flask and the preformed anion is added over the aldehyde/THF (4 mL) via canula and then, reaction allowed to warmed at room temperature overnight under magnetic stirring. Ammonium chloride (sat. aq.) added to the mixture. Extracted 3× with Ethyl Acetate. Combined organic layers washed with water (1×), with brine (1×), dried over sodium sulfate, filtered and concentrated to afford the crude material. Purification by silica gel flash chromatography (Ethyl Acetate/Heptane) provide the title compound as a yellow oil (1.33 g, 80.6%). 1H NMR (400 MHz, DMSO-d6) δ 0.83 (t, J=7.41 Hz, 3 H) 1.18-1.34 (m, 2 H) 1.46-1.57 (m, 2 H) 4.52-4.58 (m, 1 H) 5.37 (d, J=4.88 Hz, 1 H) 7.56 (dd, J=8.58, 1.95 Hz, 1 H) 7.79 (d, J=8.39 Hz, 1 H) 7.81 (d, J=2.15 Hz, 1 H); MS (M): 255.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809342B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-609ba9447418417889e15d21293a07d2 |
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| Source note | uspto-grants-2014_08 |
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