HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → [2,3-Quinoxalindiyl]bis(methylene) bisphosphonic acid tetramethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Quinoxaline | HCID 7045 | — |
| Reactant | Trimethyl phosphite | HCID 8472 | — |
| Product | [2,3-Quinoxalindiyl]bis(methylene) bisphosphonic acid tetramethyl ester | HCID 86747692 | — |
Reaction Steps
This known compound is prepared by making a solution of quinoxaline (3.16 g, 10 mmol) in hot toluene (20 ml) and treating with trimethylphosphite (2.73 g, 22 mmol). The mixture is heated at reflux temperature for 24 hours. The cooled solution deposits [2,3-quinoxalindiyl]bis(methylene) bisphosphonic acid tetramethyl ester (2.70 g, m.p. 113°-114° C.) after recrystallization from toluene. V. A. Arbuzov et al. Izvest Acad. Nauk SSSR, 1961, 1016; 1954, E 868; (Chem Abstracts (CA) 55:27352b; CA 49:13222e) report a m.p. 115°-116° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05360797 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-f34d2c28a3e748239ebc0e43af627408 |
| Source note | uspto-grants-1994_11 |