HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028198Generated: November 2, 2026
Dimethylformamide → Methyl 2-(1,4-dioxaspiro[4.5]decan-8-ylidene)acetate
https://huagongshe.com/reaction/1028198
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Trimethyl phosphonoacetate | HCID 80029 | — |
| Reactant | 1,4-Dioxaspiro[4.5]decan-8-one | HCID 567415 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | Methyl 2-(1,4-dioxaspiro[4.5]decan-8-ylidene)acetate | HCID 11063747 | 87% |
Reaction Steps
To a DMF (50 mL) solution of trimethyl phosphonoacetate (26 mL), sodium hydride (purity: 55% or higher, 7.03 g) was added in small portions at 0° C. The reaction mixture was warmed to room temperature and stirred for 30 minutes. A DMF (50 mL) solution of 1,4-cyclohexanedione monoethylene ketal (25.2 g) was added, thereto in small portions at room temperature. This suspension was stirred for 19 hours and diluted with a saturated aqueous solution of ammonium chloride, followed by two extractions with ethyl acetate. The organic layer was washed with saturated brine, then dried over sodium sulfate, and then concentrated. The residue was purified by chromatography (hexane/ethyl acetate=5:1) to obtain the title compound (29.7 g, 87%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735425B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-a38ef6477a9a4f84afccea32724e1965 |
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| Source note | uspto-grants-2014_05 |
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