Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Benzene, 1-bromo-3-(trifluoromethyl)- | HCID 9817 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (+)-Epichlorohydrin | HCID 149428 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | Sulfuric acid--ethanamine (1/1) | HCID 19907958 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 11644438 | HCID 11644438 | — |
Reaction Steps
3-Bromobenzotrifluoride (1.46 g, 6.5 mmol) was added over 5-10 minutes as a solution in diethyl ether (5 mL) dropwise to magnesium turnings (0.145 g, 5.9 mmol) in diethyl ether (2 mL), under an atmosphere of nitrogen with iodine (1 crystal) to initial reaction. The dropping funnel was washed with diethyl ether (3 mL total). The reaction was allowed to reach reflux during the addition of the bromide and then allowed to cool to room temperature and stirred for a further 1 hr. Copper (I) iodide (103 mg, 0.54 mmol) was added in one portion and the reaction mixture cooled to 0° C. over 10 minutes. (S)-epichlorohydrin (0.5 g, 5.4 mmol) was added as a solution in diethyl ether (3 mL) over 10 minutes and the reaction allowed to warm to room temperature. After 2 hrs methanol (10 mL) was added and the resulting suspension stirred vigorously. Then sodium hydroxide (1.73 g, 43 mmol) was added as a solution in water (2.7 mL), followed by more methanol (4 mL) to try to loosen the precipitate formed, and 2-aminoethane hydrogen sulfate (3.05 g, 21.6 mmol) was added. The mixture was warmed to 42° C. (bath temperature) for 2 hrs, then toluene (10 mL) and sodium hydroxide (1.35 g, crushed, 33.8 mmol) added and the resulting green paste heated at 70° C. (bath temperature) for 18 hrs. The reaction was allowed to cool to room temperature, poured into water (40 mL) and extracted with toluene (20 mL) and ethyl acetate (20 mL×2). The combined organic layers were washed with brine (10 mL), dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (silica; triethylamine/ethanol/ethyl acetate, 1/20/79 ratio) to yield the desired morpholine. The morpholine (0.27 g) was dissolved in diethyl ether (3 mL total) and added to a solution of fumaric acid (0.119 g, 1.03 mmol) in IPA (2 mL) at 40° C. and the solution allowed to cool to room temperature. The precipitate was filtered out and washed with diethyl ether and dried in vacuo to yield the desired morpholine 74 as a fumarate salt as a white powder (0.284 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07323466B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-65a76ddcecad4776a85805c540211a90 |
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| Source note | uspto-grants-2008_01 |
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