HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451597Generated: October 26, 2026
Sodium Sulfite → Diethyl 2-acetamido-2-(4-formylbutyl)malonate
https://huagongshe.com/reaction/1451597
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | Diethyl 2-acetamido-2-pentenylmalonate | HCID 57066425 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | Diethyl 2-acetamido-2-(4-formylbutyl)malonate | HCID 21849556 | — |
Reaction Steps
Diethyl 2-acetamido-2-pentenylmalonate (4.0 g) was dissolved in 210 ml of acetone and 3.3 g of N-methylmorpholine-N-oxide and 36 ml of a 1% aqueous osmium tetraoxide solution were added thereto. The mixture was stirred at room temperature for 2 hours. A solution of 700 mg of sodium sulfite in 20 ml of water was added thereto and the mixture was stirred for 15 minutes. The reaction mixture was concentrated and subjected to silica gel column chromatography using chloroform/methanol (10:1) as an eluent and a fraction having an Rf value: 0.3 (chloroform:methanol=10:1) was concentrated. The residue was dissolved in 630 ml of 1,4-dioxane and 70 ml of a 0.2M aqueous meta-sodium periodate solution was added thereto. The mixture was stirred at room temperature for 2 hours. The reaction mixture was filtrated, concentrated, extracted with ethyl acetate and washed with water. The hexane layer was dried and concentrated to give 4.17 g of colorless, oily diethyl 2-acetamido-2-(4-formylbutyl)malonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05604229 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-cd01be1585304dfcbc8ed6d14d9f9bbc |
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| Source note | uspto-grants-1997_02 |
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