HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → (2R)-6-oxohexane-1,2-diyl dinitrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | (2R)-6-hydroxyhexane-1,2-diyl dinitrate | HCID 59556786 | — |
| Catalyst | HCID 178419074 | HCID 178419074 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2R)-6-oxohexane-1,2-diyl dinitrate | HCID 86622539 | — |
Reaction Steps
Tetrapropylammonium perruthenate (16 mg, 0.05 mmol) was added to a dichloromethane (5 mL) solution of (2R)-6-hydroxyhexane-1,2-diyl dinitrate (intermediate 2, 105 mg, 0.49 mmol) and 4-methylmorpholine N-oxide (137 mg, 1.17 mmol). The solution was stirred at room temperature for 30 minutes. Water was added and the solution was extracted with dichloromethane. The combined organic layers were dried (magnesium sulfate), filtered, and concentrated in vacuo. Chromatography over silica eluting with ethyl acetate/hexanes afforded the title compound as a colorless oil. 1H NMR (500 MHz, CDCl3) δ 9.79 (s, 1H), 5.25-5.32 (m, 1H), 4.76 (dd, J=13.0, 3.5 Hz, 1H), 4.49 (dd, J=13.0, 6.5 Hz, 1H), 2.59-2.54 (m, 2H), 1.83-1.73 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07880014B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-e11987059e2043e0a297ba8fce27c009 |
| Source note | uspto-grants-2011_02 |