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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
Reactant2-NaphthylacetonitrileHCID 82008—
Solventtert-ButanolHCID 6386—
SolventMethanol tert-butyl alcoholHCID 19609033—
ProductDimethyl 3-cyano-3-(naphthalen-2-yl)hexanedioateHCID 6867300985.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877975B2
Source datasetuspto-grants-2014_11
ORD IDord-f1b69c4742fd484d851d820cc28162d0
Source noteuspto-grants-2014_11