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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729600Generated: October 30, 2026

Hydrochloric Acid → 3-(1-Methylcyclopropyl)-3-oxopropanenitrile

https://huagongshe.com/reaction/729600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantAcetonitrileHCID 6342—
ReactantTetrahydrofuranHCID 8028—
Reactanttert-Butyl methyl etherHCID 15413—
ReactantSodium SulfateHCID 24436—
ReactantEthyl 1-methylcyclopropanecarboxylateHCID 544234—
ReactantButan-1-olateHCID 12476378—
ReactantPotassium tert-butoxideHCID 23665647—
SolventMethanolHCID 887—
Product3-(1-Methylcyclopropyl)-3-oxopropanenitrileHCID 13393046—

Reaction Steps

Alternatively, to a 5 L three-necked round-bottom flask equipped with overhead stirrer, thermocouple, reflux condenser, and an addition funnel, add potassium tert-butoxide in THF (3.00 L, 3.00 moles). Mix 1-methyl-cyclopropanecarboxylic acid ethyl ester (264.00 g, 2.06 moles) with acetonitrile (123.00 g, 3.00 moles), then add through an addition funnel over 0.5 hour to the butoxide solution. Heat the resulting mixture to reflux. Reflux 2 hours, then cool to <40° C. by adding methanol (96.00 g, 3.00 mL). Stir the mixture 10 minutes, then transfer the contents to a 12 L separatory funnel containing a vigorously stirring mixture of water (3.96 L, 219.81 moles) and MTBE (3.96 L, 33.32 moles). Separate the layers and extract the aqueous layer with MTBE (3.96 L, 33.32 moles). Adjust the pH of the aqueous layer from 12.5 to 3.5 using 5 N HCl (610.00 mL, 3.05 moles). Extract the aqueous layer with MTBE (2×1.32 L, 11.11). Combine the organic layers, dry over sodium sulfate (62.00 g, 436.49 moles), and filter to afford 3-(1-methyl-cyclopropyl)-3-oxo-propionitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582638B2
Source datasetuspto-grants-2009_09
ORD IDord-0a2b97bb7f6e47499304a9445dace9fe
Source noteuspto-grants-2009_09