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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250313Generated: October 27, 2026

Methanol → Dimethyl 4-cyano-4-[3-(cyclopentyloxy)-4-methoxyphenyl]heptanedioate

https://huagongshe.com/reaction/1250313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethyl AcrylateHCID 7294—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
Reactant3-(Cyclopentyloxy)-4-methoxyphenylacetonitrileHCID 10728228—
SolventAcetonitrileHCID 6342—
ProductDimethyl 4-cyano-4-[3-(cyclopentyloxy)-4-methoxyphenyl]heptanedioateHCID 10811164—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A 12 liter round bottom flask equipped with an overhead stirrer, internal thermometer, and a reflux condensor equipped with a nitrogen inlet was flushed with nitrogen. The flask was charged with a solution of 4-cyanomethyl-2-cyclopentyloxy-1-methoxybenzene (460 g, 1.99 mol, 1.0 equivalent) in acetonitrile, and methyl acrylate (520 g, 6.0 mol, 3.0 equivalents). The contents of the flask was cooled to −10° C. A pressure equalizing addition funnel was charged with acetonitrile (1.1 L) and benzyltrimethyl ammonium hydroxide (a 40% w/w solution in methanol, 25 g, 0.06 mol, 0.03 equivalents). The contents of the addition funnel was added to the flask. An exotherm was observed, and after stirring for 30 minutes the contents of the flask were cooled to 20° C. The reaction was concentrated under reduced pressure to a residue. To the residue was added toluene (2.6 L). This solution of dimethyl-4-cyano-4-(3-cyclopentyloxy-4-methoxy-phenyl)pimelate(90% solution yield) was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337408B1
Source datasetuspto-grants-2002_01
ORD IDord-dfcd962af36d4eee88325866400cc2b9
Source noteuspto-grants-2002_01