HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732275Generated: October 26, 2026
Nitromethane → Methyl 3-methyl-4-nitrobutanoate
https://huagongshe.com/reaction/1732275
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | 1,5-Diazabicyclo(5,4,0)undec-5-ene | HCID 314112 | — |
| Reactant | Methyl Crotonate | HCID 638132 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-methyl-4-nitrobutanoate | HCID 13633418 | 66.2% |
Reaction Steps
1,5-Diazabicyclo[5,4,0]undec-5-ene (6 ml) is added to a solution of nitromethane (91.5 g) in methanol (500 ml). The resulting mixture is heated to 60° C. and methyl crotonate (100 g, 1 m) is added under nitrogen. The mixture is then stirred for 6 days at 60° C. after which it is cooled to room temperature and most of the methanol is removed in vacuo. The residue is treated with ether (500 ml) and washed with 2N hydrochloric acid (250 ml) and water (250 ml). The organic layer is dried (Na2SO4) and evaporated in vacuo to give crude product. The crude product is purified by column chromatography on silica gel (500 g, ethyl acetate/hexane 2:98) to give methyl 3-methyl-4-nitrobutanoate (106.6 g, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04237054 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-a57ec767445d4b49a721c5bb2fc48ac2 |
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| Source note | uspto-grants-1980_12 |
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