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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167019Generated: October 30, 2026

Acetic Acid → Methyl cyano(oxan-4-ylidene)acetate

https://huagongshe.com/reaction/2167019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl cyanoacetateHCID 7747—
ReactantTetrahydro-4H-pyran-4-oneHCID 121599—
ReactantAmmonium AcetateHCID 517165—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductMethyl cyano(oxan-4-ylidene)acetateHCID 11052260—

Reaction Steps

A 50 ml round-bottom flask equipped with a Dean-Stark distillation setup and condenser was charged with tetrahydro-4H-pyran-4-one (4.61 ml, 50 mmol), methyl cyanoacetate (5.3 ml, 60 mmol), ammonium acetate (1 g, 13 mmol), acetic acid (0.57 ml, 10 mmol) and benzene (30 ml). The mixture was refluxed until no more water collected in the Dean-Stark (2 hours), cooled, benzene (30 ml) added and the organic layer washed with water (50 ml). The aqueous layer was extracted with CH2Cl2 (3×50 ml). The combined organic phase was washed with sat. NaHCO3 (100 ml), brine (100 ml) dried (MgSO4), filtered and concentrated. Purified by normal phase SiO2 chromatography (10 to 60% EtOAc/hexanes) to afford methyl 2-cyano-2-(oxan-4-ylidene)acetate as a colorless oil (6.30 g, 70%, m/z: 181.1 [M+H]+ observed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09044469B2
Source datasetuspto-grants-2015_06
ORD IDord-97ca0b64904d4643bf5c5f92ccaec8b8
Source noteuspto-grants-2015_06