HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → benzofuran-2,3-dione 2-[O-(2-bromoethyl)-oxime] 3-(O-methyloxime)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 178502623 | HCID 178502623 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | benzofuran-2,3-dione 2-[O-(2-bromoethyl)-oxime] 3-(O-methyloxime) | HCID 73782576 | 70.7% |
Reaction Steps
1 g (0.0052 mol) of benzofuran-2,3-dione 3-(O-methyloxime) 2-oxime with 1.5 g (0.0141 mol) of sodium carbonate and 3 g (0.016 mol) of 1,2-dibromoethane in 5 ml of dimethylformamide are stirred at 80° C. for 6 hours. The reaction mixture is subsequently poured into water and extracted with diethyl ether. The organic phase is washed with aqueous potassium hydroxide solution and dried over sodium sulphate. The solvent is distilled off under reduced pressure, giving 1.1 g (70.7% of theory) of crude benzofuran-2,3-dione 2-[O-(2-bromoethyl)-oxime] 3-(O-methyloxime) as a mixture of stereoisomers which is reacted further without any purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06407097B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-7e4d97a86622499793133cbffb79603d |
| Source note | uspto-grants-2002_06 |