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HRID 54039作成日:2026年10月24日

Hydrochloric Acid → HCID 178447996、化合物

https://huagongshe.com/ja/reaction/54039

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物HexaneHCID 8058—
反応物4-FluoroiodobenzeneHCID 9605—
反応物ButyllithiumHCID 178418339—
反応物HCID 178447999HCID 178447999—
溶媒Diethyl EtherHCID 3283—
生成物HCID 178447996HCID 17844799640%

反応条件

温度-78 °C

反応手順

Into a 300 cc four-necked flask, 5.59 g (25.2 mmol) of 4-fluroiodobenzene and 30 cc of dry ethyl ether were charged and cooled to -78° C. Then, 17 cc (27.8 mmol) of a n-hexane solution of n--C4H9Li (1.63 mol/l) was dropwise added thereto over a period of 15 minutes. Further, the mixture was stirred at -78° C. for one hour. Then, 3.8 cc (25.5 mmol) of N,N,N',N'-tetramethylene ethylenediamine was added thereto. Further, a dry diethyl ether (10 cc) solution containing 1.3 g (6.31 mmol) of 2-(trans-4-n-propylcyclohexyl)-1,1,2-trifluoroethylene obtained in Example 1, was dropwise added thereto over a period of 30 minutes. Further, the mixture was reacted at the same temperature for one hour, and then stirred at room temperature for one hour. Then, 50 cc of 1N hydrochloric acid was added thereto. The organic layer was separated. The aqueous layer was extracted with n-hexane, and the extract was combined with the organic layer. The combined organic layer was washed with water and dried. Further, the solvent was distilled off. The obtained crude solution was purified by silica gel column chromatography to obtain a solid. This solid was recrystallized from methanol to obtain 0.71 g (yield: 40%) of (E)-1-(4-fluorophenyl)-2-(trans-4-n-propylcyclohexyl)-1,2-difluoroethylene.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05621147
出典データセットuspto-grants-1997_04
ORD IDord-c38ba36af653435db6a9be5af49de60e
出典メモuspto-grants-1997_04