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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626479Generated: October 30, 2026

Acetic Acid → Methyl 2-cyano-2-(6-oxaspiro[4.5]decan-9-ylidene)acetate

https://huagongshe.com/reaction/626479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl cyanoacetateHCID 7747—
ReactantAmmonium AcetateHCID 517165—
Reactant6-Oxaspiro[4.5]decan-9-oneHCID 64106463—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductMethyl 2-cyano-2-(6-oxaspiro[4.5]decan-9-ylidene)acetateHCID 68313883—

Reaction Steps

A 100 ml round-bottom flask equipped with a Dean-Stark distillation setup and condenser was charged with 6-oxaspiro[4.5]decan-9-one (6 g, 39 mmol, which was prepared according to Hanschke, E. Chem. Ber. 1955, 88, 1053), methyl cyanoacetate (4.1 ml, 46.7 mmol), ammonium acetate (780 mg, 10.1 mmol), acetic acid (0.44 ml, 7.8 mmol) and benzene (40 ml). The mixture was refluxed until no more water collected in the Dean-Stark (2 hours), cooled, benzene (30 ml) added and the organic 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 (7% to 60% EtOAc/hexanes) to give methyl 2-cyano-2-[(9Z)-6-oxaspiro[4.5]decan-9-ylidene]acetate as a colorless oil (8.93 g, 97.5%, m/z 235.1 [M+H]+ observed).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309234B2
Source datasetuspto-grants-2016_04
ORD IDord-d82dda1b1692478984e4a350e4353dd2
Source noteuspto-grants-2016_04