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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227341Generated: October 25, 2026

Hydracrylonitrile → 1-[(2-Cyanoethoxycarbonyl)methyl]-1-Cyclohexane Acetic Acid

https://huagongshe.com/reaction/227341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydracrylonitrileHCID 8011—
Reactant1,1-Cyclohexanediacetic AnhydrideHCID 2734289—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-[(2-Cyanoethoxycarbonyl)methyl]-1-Cyclohexane Acetic AcidHCID 2234096095%

Reaction Conditions

Temperature30 °C

Reaction Steps

8.2 mL of 1.6M butyllithium was added to a −78° C. solution of 3-hydroxy-propionitrile (13.19 mmol) in 50 mL of THF. The reaction mixture was warmed to 30° C. and stirred for 30 minutes. Then, a solution of 1,1-cyclohexanediacetic anhydride (10.99 mmol) in 10 mL of THF was added dropwise. The reaction mixture was warmed to room temperature over a period of one hour and stirred at room temperature with monitoring by TLC. When the reaction was judged complete, the reaction mixture was quenched with saturated ammonium chloride solution and THF was removed under reduced pressure. The aqueous layer was extracted with ethyl acetate, washed with brine and dried over Na2SO4. After concentration in vacuo the residue was purified on silica gel (5% methanol in dichloromethane) to afford 2.64 g (95%) of the title compound. 1H NMR (CDCl3): δ 4.28 (2H, t, J=6.4 Hz); 2.71 (2H, t, J=6.4 Hz); 2.61 (4H, m); 1.52-1.42 (10H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560483B2
Source datasetuspto-grants-2009_07
ORD IDord-14a017c53a274a38a7fe18852d35e6ba
Source noteuspto-grants-2009_07