HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydracrylonitrile → ethyl N-carbobenzoxy-N-[bis(beta-cyanoethoxy)phosphonomethyl]glycinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydracrylonitrile | HCID 8011 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | ethyl N-carbobenzoxy-N-(dichlorophosphonomethyl)glycinate | HCID 54297302 | — |
| Product | ethyl N-carbobenzoxy-N-[bis(beta-cyanoethoxy)phosphonomethyl]glycinate | HCID 23332172 | — |
Reaction Steps
Ethyl N-carbobenzoxy-N-(dichlorophosphonomethyl)glycinate (11.7 g., 0.032 mole) and 2-cyanoethanol (4.52 g., 0.064 mole) were dissolved in tetrahydrofuran (50 ml). To this solution was added triethylamine (6.42 g., 0.064 mole) dissolved in 25 ml. of tetrahydrofuran. The resultant solution was stirred overnight at room temperature. The reaction mixture was then filtered and the filtrate concentrated in vacuo to yield ethyl N-carbobenzoxy-N-[bis(β-cyanoethoxy)phosphonomethyl]glycinate as a yellow oil, ND25 =1.05 and having the following analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04231782 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-e13ee0364e1244808fb144af690deaa4 |
| Source note | uspto-grants-1980_11 |