HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646174Generated: October 25, 2026
Diethyl vinylphosphonate → HCID 19801586, compound
https://huagongshe.com/reaction/1646174
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl vinylphosphonate | HCID 69629 | — |
| Reactant | Ethyl 2-((3-bromophenyl)amino)acetate | HCID 302657 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 19801586 | HCID 19801586 | 60.5% |
Reaction Steps
A solution of ethyl N-(3-bromophenyl)glycinate (Example B) (4 g, 15.5 mmol), diethyl vinylphosphonate (4.92 g, 30 mmol), and bis(triphenylphosphine) palladium (II) chloride (1 g) in dimethylformamide (15 ml) and triethyamine (5 ml) is immersed in an oil bath (95° C.) and stirred for 20 hours. After cooling the dimethylformamide is removed in vacuo and the oily brown residue is dissolved in a saturated solution of sodium chloride and extracted with chloroform. The chloroform layer is dried over magnesium sulfate, filtered and evaporated to give a residue (3.2 g). Purification is accomplished by silica gel chromatography (ethyl acetate as eluant, a single fluorescent spot on tlc, Rf=0.5 (ethyl acetate)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05179085 |
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| Source dataset | uspto-grants-1993_01 |
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| ORD ID | ord-46158ea397104952ba56d989571bf4a3 |
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| Source note | uspto-grants-1993_01 |
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