HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76222Generated: October 29, 2026
Acetic Acid → Methyl 2-cyano-2-(6-oxaspiro[4.5]decan-9-ylidene)acetate
https://huagongshe.com/reaction/76222
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methyl cyanoacetate | HCID 7747 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 6-Oxaspiro[4.5]decan-9-one | HCID 64106463 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 2-cyano-2-(6-oxaspiro[4.5]decan-9-ylidene)acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835488B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-1a08ef7158b248468d7d9c73e9d2df4f |
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| Source note | uspto-grants-2014_09 |
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