HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157741Generated: October 30, 2026
Triethyl phosphonoacetate → HCID 178471800, compound
https://huagongshe.com/reaction/1157741
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-oxocyclohexanecarboxylate | HCID 317638 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | Ethanol sodium ethoxide | HCID 23706232 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178471800 | HCID 178471800 | — |
Reaction Steps
To a solution (600 ml) of ethyl 4-oxocyclohexanecarboxylate (150 g) in ethanol was added sodium hydroxide (38.8 g) with stirring at room temperature. The reaction solution was stirred for 1 hr and ethyl diethylphosphonoacetate (192 ml) was added. To this reaction solution was added dropwise 21% sodium ethoxide/ethanol solution (363 ml) with stirring under ice-cooling over 1 hr. The stirring was continued for 1 hr and acetic acid (126 ml) was added. Then ammonium formate (111 g) and palladium carbon (5%, 15 g) were added and the mixture was stirred at 60° C. for 6 hr with heating. The reaction solution was allowed to return to room temperature and insoluble materials were filtered off through celite. The filtrate was concentrated and the obtained residue was diluted with ethyl acetate. The mixture was washed successively with 2N aqueous hydrochloric acid, water and saturated brine. The organic layer was dried over sodium sulfate and sodium sulfate was filtered off. The filtrate was concentrated to give a crudely purified product (180.4 g) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807701B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-5ce172b7b45740f4830bf7f1241b9726 |
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| Source note | uspto-grants-2010_10 |
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