HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → dibenzyl E-2-amino-4-phosphonomethyl-hept-3-ene-1,7-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | diethyl E-2-amino-4-phosphonomethyl-hept-3-ene-1,7-dicarboxylate | HCID 86746004 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | dibenzyl E-2-amino-4-phosphonomethyl-hept-3-ene-1,7-dicarboxylate | HCID 67900429 | — |
Reaction Steps
To 3.25 g (10 mmol) of diethyl E-2-amino-4-phosphonomethyl-hept-3-ene-1,7-dicarboxylate and 10.8 g (100 mmol) of benzyl alcohol are added 10 ml of methylene chloride and 20 ml of 4N ethereal hydrochloric acid, and the mixture is allowed to stand for 1 week. The mixture is then evaporated to dryness, and the residue is dissolved in 25 ml of ethanol. To this solution is then added dropwise a solution of 15 ml of propylene oxide in 15 ml of ethanol. The readily volatile constituents are removed by evaporation under reduced pressure, affording dibenzyl E-2-amino-4-phosphonomethyl-hept-3-ene-1,7-dicarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05134134 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-11b9f31957fd49278d2f7b588abfdae7 |
| Source note | uspto-grants-1992_07 |