HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-[3-(1-Ethoxyethoxy)-4,4,4-trifluorobutoxy]-4-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Chloro-4-nitrobenzene | HCID 7474 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 542222 | HCID 542222 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[3-(1-Ethoxyethoxy)-4,4,4-trifluorobutoxy]-4-nitrobenzene | HCID 19773690 | 78% |
Reaction Steps
To a suspension of 2.4 g (0.049 mol) of 50% NaH in 50 ml of THF, is slowly added a solution of 10.6 g (0.049 mol) of 3-(1-ethoxyethoxy)-4,4,4-trifluoro-1-butanol in 15 ml of THF. When no more gas evolves, a solution of 6.5 g (0.041 mol) of 4-chloronitrobenzene in 65 ml of DMF is added. After 30 min., the reaction medium is poured on iced water. The reaction medium is extracted with ether. The organic phase is washed with water, dried over Na2SO4 and concentrated. The aimed product is obtained with a 78% yield after recrystallization from isopropanol. m.p.: 81° C.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05036091 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-e1f86762990048cdbb45541973adff16 |
| Source note | uspto-grants-1991_07 |