HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594328Generated: October 26, 2026
Dichloromethane → HCID 13218106, compound
https://huagongshe.com/reaction/594328
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Ethyl 2-methyl-4-pentenoate | HCID 62024 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13218106 | HCID 13218106 | — |
Reaction Steps
A colorless solution of ethyl 2-methylpent-4-enoate (5.000 g; 35.16 mmol) in dioxane (260 ml) and water (85 ml) was treated successively with 2,6-lutidine (7.536 g; 70.32 mmol), a solution of osmium tetroxide (2.5 wt. % in 2-methylpropan-2-ol; 0.45 ml), and NaIO4 (30.083 g; 140.65 mmol). The resulting beige heterogeneous reaction mixture was further stirred at rt, under nitrogen, for 20.5 h. The resulting milky mixture was treated with water (100 ml) and DCM (500 ml). The layers were separated, and the aq. layer was further extracted with DCM (200 ml/150 ml). The mixed slightly yellow organic layers were then washed with brine (200 ml), dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure to give crude ethyl 2-methyl-4-oxobutanoate as a dark-yellow/slightly brown oil which was directly used for the next step without additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242970B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-7d1c42c77f7b468184513b6c8b75b7ad |
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| Source note | uspto-grants-2016_01 |
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