HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728878Generated: October 30, 2026
Ethanol → 1-Ethyl (3E)-2-amino-4-methyl-5-phosphono-3-pentenoate
https://huagongshe.com/reaction/728878
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | HCID 86745094 | HCID 86745094 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Ethyl (3E)-2-amino-4-methyl-5-phosphono-3-pentenoate | HCID 6372334 | — |
Reaction Steps
56.7 ml of trimethylbromosilane are added dropwise within a period of 15 minutes at 20° to a solution of 25.42 g of E-2-formylamino-4-methyl-5-diisopropylphosphono-3-pentenoic acid ethyl ester in 102 ml of dry dichloromethane. After stirring at room temperaturefor 20 hours, 102 ml of ethanol are added dropwise within a period of 15 minutes, and the whole is stirred for a further 20 hours. The clear reaction solution is then completely concentrated by evaporation in vacuo.The residue is concentrated by evaporation a further three times in each case after the addition of 100 ml of toluene. The oily residue is dissolved in 102 ml of ethanol, and a solution of 102 ml of propylene oxide in 102 ml of ethanol is added dropwise thereto. The product, obtained in crystalline form, is filtered off after 2 hours (room temperature) and washed with ethanol and ether. After drying (80°, 4 hours) under a high vacuum, E-2-amino-4-methyl-5 -phosphono-3-pentenoic acid ethyl ester is obtained in analytically pure form, m.p. 212° (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-27d07e4db5bf4ba1ab26cc9733d6e123 |
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| Source note | uspto-grants-1991_09 |
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