Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 57801040 | HCID 57801040 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Solvent | Sodium borohydride | HCID 4311764 | — |
| Product | HCID 11484593 | HCID 11484593 | — |
Reaction Steps
4-(1-pentyloxyhex-5-enyl)-biphenyl (1 g) was dissolved in 0.5 M NaBH4 in diglyme (8 ml) and chilled in an ice bath. BF3.OEt2 (1 ml) in diglyme (4 ml) was added with vigorous stirring. Stirring was continued for 1 hour and water (1 ml) was added. 3M NaOH (2 ml) was added followed by 30% H2O2 (3 ml). Anhydrous K2CO3 (5 g) was added and the solvent decanted. The K2CO3 was washed with ethyl acetate and the combined organics dried (Na2SO4) and evaporated. Distillation under vacuum removes most of the remaining diglyme. The residue was purified by column chromatography (ethyl acetate/petrol) to give an oil. δC (CDCl3, 62.9 MHz): 14.1, 22.6, 25.7, 25.8, 28.4, 29.7, 32.7, 34.4, 63.0, 69.0, 82.0, 126.9, 127.1, 127.2, 128.8, 140.2, 141.0 and 142.4. δH (CDCl3, 250 MHz): 0.88 (3H, m), 1.16-1.55 (14H, m), 3.30 (2H, m), 3.62 (2H, t, J 6.1), 4.21 (1H, t, J 6.1), 7.34 (3H, d, J 7.6), 7.43 (2H, t, J 7.3) and 7.58 (4H, t, J 7.3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07598289B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-6471a3ec7b334709a6c7a5e6ad7d6304 |
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| Source note | uspto-grants-2009_10 |
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