Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | HCID 9858056 | HCID 9858056 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 9969884 | HCID 9969884 | 72% |
Reaction Steps
To a solution of 4.5 g of alcohol 8 250 mL of dry ethyl ether in an ice bath was added dropwise of 1.7 mL of phosphorous tribromide. After stirring for 3 days in an ice bath, 0.5 mL of conc. hydrobromic acid was added to this mixture. The resulting solution was stirred continuously at room temperature overnight, and 100 mL of ice was added to quench the reaction. The white solid was collected, dissolved in ethyl acetate, washed with saturated sodium hydrocarbonate solution and saturated brine. The organic layer was filtered through a silica gel pad. After the solvent evaporated, the crude solid was recrystallized from ethyl acetate and hexanes to form 3.8 g of the title compound as a white solid (72% yield, >95% de): mp 156.5-157.5 ° C.; [α]25D=−38.2 (c 1.0, CH3OH); 1H NMR (200 MHz, CDCl3) δ 7.40-7.10 (m, 7 H), 6.99 (m, 2 H), 5.52 (br d, J=7.6 Hz, 1 H), 4.98 (m, 1 H), 3.35-3.20 (m, 2 H), 3.05 (m, 1 H), 2.51 (dd, J=6.3, 14.0 Hz, 1 H), 2.37 (dd, J=8.7, 14.0 Hz, 1 H), 2.25-2.05 (m, 2 H), 1.25 (d, J=6.9 Hz, 3 H); 13C NMR (125 MHz, CDCl3) δ 169.7, 161.8, 142.8, 137.7, 129.1, 128.6, 127.4, 126.1, 115.7, 48.6, 44.0, 40.6, 38.7, 30.9, 21.3. Anal. Calcd for C19H21BrFNO: C, 60.33; H, 5.60; N, 3.70. Found: C, 60.57; H, 5.54; N, 3.82.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06833458B2 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-322a08148f1f4c74a18571ae401d7297 |
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| Source note | uspto-grants-2004_12 |
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