HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Dimethyl 3-benzyl-2-isoxazolin-5-ylphosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Dimethyl vinylphosphonate | HCID 78376 | — |
| Reactant | 1-Nitro-2-phenylethane | HCID 80208 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Dimethyl 3-benzyl-2-isoxazolin-5-ylphosphonate | HCID 20062388 | — |
Reaction Steps
13.5 ml (0.124 mol) of phenyl isocyanate, 9.5 g (0.07 mol) of dimethyl vinylphosphonate and 1 ml of triethylamine are introduced into 120 ml of toluene. A solution of 9.3 g (0.062 mol) of 2-phenylnitroethane and 1 ml of triethylamine dissolved in 150 ml of toluene is added dropwise in 5 hours, the mixture is stirred overnight and then for 30 minutes after addition of 30 ml of concentrated aqueous ammonia, precipitated diphenylurea is removed by filtration and washed with ethyl acetate, and the combined organic phases are extracted by shaking successively with water, 2 N hydrochloric acid and water, and are dried and concentrated. 13.9 g of reddish brown oil remain.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05006515 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-64ce610377564b8b98bef1e464548e59 |
| Source note | uspto-grants-1991_04 |