HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728879Generated: October 30, 2026
Ethanol → 1-Ethyl (3E)-2-amino-4-methyl-5-phosphono-3-pentenoate
https://huagongshe.com/reaction/728879
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | HCID 21612902 | HCID 21612902 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Ethyl (3E)-2-amino-4-methyl-5-phosphono-3-pentenoate | HCID 6372334 | — |
Reaction Steps
16.9 g of E-2-formylamino-4-methyl-5-dimethylphosphono-3-pentenoic acid ethyl ester are dissolved in 80 ml of dichloromethane under a nitrogen atmosphere, and 30 ml of trimethylbromosilane are added dropwise at approximately 25° within a period of 30 minutes. The mixture is stirred at room temperature for 20 hours, and then 80 ml of ethanol are added dropwise at approximately 25° within a period of 30 minutes. The mixture is then again stirred at room temperature for 22 hours and is then concentrated by evaporation. The residue is dissolved in 80 ml of ethanol, and 80 ml of propylene oxide in 80 ml of ethanol are added dropwise with slight cooling. The mixture is stirred at room temperature for one hour to complete the reaction, filtered and washed with ethanol and ether. In this manner there is obtained E-2-amino-4-methyl-5-phosphono-3-pentenoic acid ethyl ester, m.p. 215°-217° (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05051413 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-2390e1f7c9db4f64bac82d9127794d19 |
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| Source note | uspto-grants-1991_09 |
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