Bis(2-ethylhexyl) 4-cyclohexene-1,2-dicarboxylate

Conditions: temp:81.51; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: In the stream of an argon gas, 80 g of 4-cyclohexene-1,2-dicarboxylic di(2-ethylhexyl)ester (manufactured by Tokyo Chemical Industry Co., Ltd.) and 900 mL of isopropyl alcohol was placed. 660 mL of an aqueous solution of 42.3 g of sodium hydrogen sulfite (manufactured by Wako Pure Chemical Industries, Ltd.) was added. The resulting solution was heated to a reflux temperature, and stirred at 80 to 83° C. for 16 hours. During this stirring, every one hour from the start to 1 to 5 hours after the start of refluxing, as well as after 9 hours and 10 hours, 1.66 g of 2,2′-azobis(isobutyronitrile) (manufactured by Wako Pure Chemical Ltd.) was added. After cooling to room temperature, the reaction liquid was concentrated under reduced pressure. The resulting solution was heated to a reflux temperature During this stirring, every one hour from the start to 1 to 5 hours after the start of refluxing as well as after 9 hours After cooling to room temperature the reaction liquid was concentrated under reduced pressure

Conditions: temp:81.51; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: In the stream of an argon gas, 80 g of 4-cyclohexene-1,2-dicarboxylic di(2-ethylhexyl)ester (manufactured by Tokyo Chemical Industry Co., Ltd.) and 900 mL of isopropyl alcohol was placed. 660 mL of an aqueous solution of 42.3 g of sodium hydrogen sulfite (manufactured by Wako Pure Chemical Industries, Ltd.) was added. The resulting solution was heated to a reflux temperature, and stirred at 80 to 83° C. for 16 hours. During this stirring, every one hour from the start to 1 to 5 hours after the start of refluxing, as well as after 9 hours and 10 hours, 1.66 g of 2,2′-azobis(isobutyronitrile) (manufactured by Wako Pure Chemical Ltd.) was added. After cooling to room temperature, the reaction liquid was concentrated under reduced pressure. The resulting solution was heated to a reflux temperature During this stirring, every one hour from the start to 1 to 5 hours after the start of refluxing as well as after 9 hours After cooling to room temperature the reaction liquid was concentrated under reduced pressure

Conditions: temp:81.51; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: In the stream of an argon gas, 80 g of 4-cyclohexene-1,2-dicarboxylic di(2-ethylhexyl)ester (manufactured by Tokyo Chemical Industry Co., Ltd.) and 900 mL of isopropyl alcohol was placed. 660 mL of an aqueous solution of 42.3 g of sodium hydrogen sulfite (manufactured by Wako Pure Chemical Industries, Ltd.) was added. The resulting solution was heated to a reflux temperature, and stirred at 80 to 83° C. for 16 hours. During this stirring, every one hour from the start to 1 to 5 hours after the start of refluxing, as well as after 9 hours and 10 hours, 1.66 g of 2,2′-azobis(isobutyronitrile) (manufactured by Wako Pure Chemical Ltd.) was added. After cooling to room temperature, the reaction liquid was concentrated under reduced pressure. The resulting solution was heated to a reflux temperature During this stirring, every one hour from the start to 1 to 5 hours after the start of refluxing as well as after 9 hours After cooling to room temperature the reaction liquid was concentrated under reduced pressure