Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707530Generated: October 30, 2026

N-methyl-2-pyrrolidone → HCID 178448078, compound

https://huagongshe.com/reaction/1707530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant2-(4'-Bromo-3',5'-difluorophenyl)-5-(4'-propylcyclohexyl)-1,3-dioxaneHCID 18961533—
ProductHCID 178448078HCID 178448078—

Reaction Steps

7.3 g (0.018 mol) of 2-(4'-bromo-3',5'-difluorophenyl)-5-(4'-propylcyclohexyl)-1,3-dioxane, 2.5 g (0.027 mol) of CuCN2 and 54 cm3 of NMP were refluxed for 2 hours with a mantle heater. After cooling the reactant to room temperature, 40 cm3 of EDA was added, it was poured into 50 cm3 of ice water, extracted with chloroform and washed with an aqueous EDA solution and water. The chloroform was removed, and the residue was dissolved in hexane and washed with water to remove the NMP. The hexane was removed, and the residue was treated in a silica gel column with chloroform as the solvent. The chloroform was removed, and the residue was repeatedly recrystallized in a solvent mixture of acetone and methanol until there were no cis forms to obtain 1.4 g (0.004 mol) of trans-2-(4'-cyano-3',5'-difluorophenyl)-5-(trans-4'-propylcyclohexyl)-1,3-dioxane. The phase transition temperature of this compound was measured with DSC as follows. ##STR17## (here, C shows crystals, N shows the nematic phase and I shows isotropic liquid.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05354502
Source datasetuspto-grants-1994_10
ORD IDord-40893ff6e4ea4a2b95a175bd828872bc
Source noteuspto-grants-1994_10