HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400159Generated: November 1, 2026
Triethyl phosphonoacetate → HCID 86749011, compound
https://huagongshe.com/reaction/2400159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Farnesyl bromide | HCID 550199 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86749011 | HCID 86749011 | 45.3% |
Reaction Steps
0.59 g of 55% sodium hydride was suspended in 5 ml of N,N-dimethylformamide in a nitrogen atmosphere, followed by the dropwise addition thereto of 5 ml of a solution of 3.0 g of ethyl diethylphosphonoacetate in N,N-dimethylformamide at room temperature. The obtained mixture was stirred for 10 minutes. 5 ml of a solution of 4.5 g of farnesyl bromide in N,N-dimethylformamide was added to the resulting mixture at room temperature. The obtained mixture was further stirred for one hour, followed by the addition thereto of ice-water. The resulting mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of common salt, dried over anhydrous magnesium sulfate and distilled in a vacuum to remove the solvent. The obtained crude product was purified by silica gel column chromatography (solvent: n-hexane/ethyl acetate) to give 2.6 g of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05453524 |
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| Source dataset | uspto-grants-1995_09 |
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| ORD ID | ord-52259956dc9b4945ab8b48f44eec31ae |
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| Source note | uspto-grants-1995_09 |
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