HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexane → p-Methoxybenzyl alpha-amino-dimethylphosphonoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | p-methoxybenzyl N-benzylidene-alpha-amino-dimethylphosphonoacetate | HCID 54064440 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | p-Methoxybenzyl alpha-amino-dimethylphosphonoacetate | HCID 21529965 | — |
Reaction Steps
p-Methoxybenzyl N-benzylidene-α-amino-dimethylphosphonoacetate (9.78 g) in ether (50 ml) is added over 20 minutes to a stirring solution of p-toluenesulfonic acid monohydrate (4.76 g) in ether (150 ml). Cyclohexane (100 ml) is added and the solvents are decanted off. The residue is washed with more 2:1 ether-cyclohexane, which is again decanted off. The residue is partitioned between methylene chloride and 1 M dipotassium hydrogen phosphate (50 ml). The organic portion is separated, washed with water, dried, and evaporated in vacuo to give p-methoxybenzyl α-aminodimethylphosphonoacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03962224 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-68f825aa3f964ab7a444afb4f4d7046b |
| Source note | uspto-grants-1976_06 |