Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 22492558 | HCID 22492558 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57572811 | HCID 57572811 | 89.2% |
Reaction Steps
To a 50 mL flask containing 6-propylnonan-1-ol (4.92 g, 26.4 mmol) was added hydrobromic acid 48% (12 mL, 105.6 mmol, 4 eq.) and conc. sulfuric acid (1.4 mL, 26.4 mmol, 1 eq.) and the mixture was heated to reflux (95° C.) for 14 h. The reaction was cooled to room temperature before adding H2O (40 mL). The mixture was extracted with dichloromethane (3×120 mL) and the combined organic phases were washed with aqueous sodium bicarbonate (40 mL, 1M). Drying over magnesium sulfate and evaporation gave 1-bromo-6-propylnonane (5.87 g, 89% yield) as a brown liquid. 1H NMR (CDCl3, 400 MHz) d?(ppm): 3.40 (t, J=6.8 Hz, 2H); 1.86 (tt, J=6.8 Hz, J=6.8 Hz, 2H); 1.45-1.35 (m, 2H); 1.34-1.15 (m, 13H); 0.88 (t, J=6.8 Hz, 6H). 13C NMR (CDCl3, 129.9 MHz) d?(ppm): 36.9; 36.0 (2C); 34.0; 33.5; 33.9; 28.7; 25.8; 19.8 (2C); 14.5 (2C).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893258B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-1bb6f9d15d5544908871abb6cbfd0d72 |
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| Source note | uspto-grants-2011_02 |
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