HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215433Generated: October 30, 2026
N-Methylmorpholine N-oxide monohydrate → HCID 21948859, compound
https://huagongshe.com/reaction/2215433
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylmorpholine N-oxide monohydrate | HCID 2724197 | — |
| Reactant | HCID 21948811 | HCID 21948811 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 21948859 | HCID 21948859 | — |
Reaction Steps
336 mg (2.5 mmol) of N-methylmorpholine-N-oxide hydrate and 10.22 ml of osmium tetroxide solution in isopropanol are added at 0° C. to a solution that consists of 3.18 g (15.88 mmol) of 5-nitro-2-vinylquinoline in 140 ml of acetone and 21 ml of water, and the reaction mixture is stirred for 24 hours at room temperature. Then, the solvent is removed in a vacuum, and the residue is taken up in ethyl acetate. The organic phase is washed with water and saturated sodium chloride solution. The aqueous phase is extracted repeatedly with dichloromethane, diethyl ether and ethyl acetate. The combined organic phases are dried on sodium sulfate. After removal of the solvent and purification of silica gel with hexane-ethyl acetate (0–100%) as well as with ethyl acetate-methanol (0–20%), 1.64 g (44% of theory) of the product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07109212B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-7a5e1a900e3a456f930918cf3e006970 |
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| Source note | uspto-grants-2006_09 |
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