Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 18624262 | HCID 18624262 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 18624266 | HCID 18624266 | 82% |
Reaction Steps
A solution of 2-(3-ethylphenyl)-2-adamantanol (1.82 g, 7.14 mmol) in dry CHCl3 (5 mL) under argon, was treated with trimethylsilyl cyanide (1.00 mL, 7.5 mmol), cooled to 0° C., treated with BF3 etherate (1.10 mL, 8.57 mmol), allowed to warm to room temperature and stirred for 2 h. The mixture was treated with dilute NaHCO3 (10 mL), extracted with CHCl3 (2×10 mL), the combined extracts washed with water (10 mL), dried (MgSO4), concentrated in vacuo and purified by chromatography [SiO2; heptane-EtOAc (9:1)] to give the product (1.54 g, 82%) as a colourless oil: IR νmax (thin film)/cm−1 2922, 2860, 2226, 1604, 1487, 1453, 1105, 799 and 704; NMR δH (400 MHz, CDCl3) 1.24 (3H, t, J 7.5 Hz), 1.62-1.65 (2H, m), 1.70-1.82 (5H, m), 1.98-204 (3H, m), 2.45-2.48 (2H, m), 2.66 (2H, q, J 7.5 Hz), 2.79 (2H, s), 7.15 (1H, d, J 7.5 Hz) and 7.25-7.34 (3H, m); Anal. Calcd for C19H23N: C, 85.99; H, 8.73; N, 5.28. Found: C, 85.85; H, 8.77; N, 5.23.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06531511B1 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-cde2e1f205264a15b1ab816767dd6625 |
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| Source note | uspto-grants-2003_03 |
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