HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333279Generated: October 25, 2026
Methyl Acrylate → Dimethyl 3-cyano-3-(naphthalen-2-yl)hexanedioate
https://huagongshe.com/reaction/333279
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Acrylate | HCID 7294 | — |
| Reactant | 2-Naphthylacetonitrile | HCID 82008 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Methanol tert-butyl alcohol | HCID 19609033 | — |
| Product | Dimethyl 3-cyano-3-(naphthalen-2-yl)hexanedioate | HCID 68673009 | 85.8% |
Reaction Steps
2-naphthylacetonitrile (3.45 g, 20.6 mmol) and methyl acrylate (9.7 ml, 107 mmol) were suspended in 2-methyl-2-propanol (10 ml). Heat was applied to the reaction vessel until the solution became clear. The mixture was cooled to room temperature, at which time (Bu)4NOH (6.9 mmol, 0.33 equiv.) was added as a solution in 2-methyl-2-propanol:methanol (1:2). The combined reaction mixture was heated to reflux for 4 h under vigorous stirring at which time the reaction appeared complete by GC-MS. After allowing the reaction to cool the mixture was partitioned between H2O (75 ml) and EtOAc (50 ml). The aqueous layer was removed and washed with EtOAc (2×50 ml). The combined organic phases were washed with NaHCO3 (sat. aq.) and brine and dried over MgSO4. After filtration the solvent was removed in vacuo. The crude product was purified by flash column chromatography (25% EtOAc in hexanes) to isolate the title compound as a light yellow oil (5.75 g, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877975B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-f1b69c4742fd484d851d820cc28162d0 |
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| Source note | uspto-grants-2014_11 |
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