Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | (R)-4-(6-hydroxy-5-(trifluoromethyl)naphthalen-2-yl)-4-methyloxazolidin-2-one | HCID 46196301 | — |
| Reactant | HCID 178445811 | HCID 178445811 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178445733 | HCID 178445733 | 30.5% |
Reaction Steps
The mixture of cis-4-tert-butylcyclohexanol (30.4 mg, 0.000195 mol), (R)-4-(6-hydroxy-5-(trifluoromethyl)naphthalen-2-yl)-4-methyloxazolidin-2-one (50.5 mg, 0.000162 mol) and triphenylphosphine (51.1 mg, 0.000195 mol) in tetrahydrofuran (2 mL, 0.02 mol) was heated to reflux, and diisopropyl azodicarboxylate (0.0383 mL, 0.000195 mol) was is added dropwise and was stirred and refluxed for 3 hours. The mixture was taken up into methylene chloride and subjected to chromatography purification with EtOAc/hexane (10:90 to 80:20) to give product (R)-4-(6-(trans-4-tert-butylcyclohexyloxy)-5-(trifluoromethyl)naphthalen-2-yl)-4-methyloxazolidin-2-one (22.2 mg, 30%). LCMS: Rf=2.41 min (450.46, M+1, 70%; 491.47, M+ACN, 100%). 1H NMR (400 MHz, CHLOROFORM-d) δ=8.25 (dd, J=8.7, 1.4 Hz, 1H), 7.91 (d, J=9.0 Hz, 1H), 7.79 (d, J=2.0 Hz, 1H), 7.52 (dd, J=9.3, 2.3 Hz, 1H), 7.34 (d, J=9.3 Hz, 1H), 5.98 (br. s., 1H), 4.45 (d, J=8.6 Hz, 1H), 4.41 (d, J=8.6 Hz, 1H), 4.38-4.26 (m, 1H), 2.19 (d, J=13.1 Hz, 2H), 1.89 (d, J=10.0 Hz, 2H), 1.87 (s, 3H), 1.59-1.48 (m, 2H), 1.21-1.05 (m, 3H), 0.89 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546359B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-8a1519228f414649a188d43bdb017190 |
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| Source note | uspto-grants-2013_10 |
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