Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087609Generated: November 1, 2026

Water → 1-[3-(1-Ethoxyethoxy)-4,4,4-trifluorobutoxy]-4-nitrobenzene

https://huagongshe.com/reaction/1087609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Chloro-4-nitrobenzeneHCID 7474—
ReactantSodium hydrideHCID 24758—
ReactantHCID 542222HCID 542222—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product1-[3-(1-Ethoxyethoxy)-4,4,4-trifluorobutoxy]-4-nitrobenzeneHCID 1977369078%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05036091
Source datasetuspto-grants-1991_07
ORD IDord-e1f86762990048cdbb45541973adff16
Source noteuspto-grants-1991_07