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HRID 363457作成日:2026年10月27日

Dimethyl Sulfide → trans-6-pentafluoroethyl-2,2-bisfluoromethyl-3,4-dihydro-4-(3-oxo-cyclopent-1-enyloxy)-2H-1-benzopyran-3-ol

https://huagongshe.com/reaction/363457

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfideHCID 1068—
反応物Sulfuric AcidHCID 1118—
反応物Sodium hydrideHCID 24758—
反応物1,3-CyclopentanedioneHCID 77466—
反応物3,4-epoxy-6-pentafluoroethyl-2,2-bisfluoromethyl-3,4-dihydro-2H-1-benzopyranHCID 15871792—
触媒copper(I) bromideHCID 24593—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物trans-6-pentafluoroethyl-2,2-bisfluoromethyl-3,4-dihydro-4-(3-oxo-cyclopent-1-enyloxy)-2H-1-benzopyran-3-olHCID 867506143.4%

反応条件

温度-20 °C

反応手順

In 40 ml of tetrahydrofuran was dissolved 0.36 g of cyclopentan-1,3-dione and 0.13 g of sodium hydride (60%) was added thereto under nitrogen stream with cooling at -20° C. After the mixture was stirred at room temperature for 15 minutes, 0.72 g of a complex of copper (I) bromide and dimethyl sulfide was added. To the reaction mixture was added 0.92 g of 3,4-epoxy-6-pentafluoroethyl-2,2-bisfluoromethyl-3,4-dihydro-2H-1-benzopyran dissolved in 10 ml of tetrahydrofuran. The mixture was stirred for 6 days. To the mixture were added water and a small amount of concentrated sulfuric acid. The mixture was extracted with methylene chloride and the organic layer was washed with water and dried. The solvent was distilled off and the resultant residue was purified using silica gel column chromatography (developing solution, MeOH:CH2Cl2 =1:99) and another silica gel column chromatography (developing solution, AcOEt:hexane=1:1) to obtain 0.04 g of trans-6-pentafluoroethyl-2,2-bisfluoromethyl-3,4-dihydro-4-(3-oxo-cyclopent-1-enyloxy)-2H-1-benzopyran-3-ol represented by the following formula having a melting point of 165°-167° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05874446
出典データセットuspto-grants-1999_02
ORD IDord-1fbfe959989745e5821f9fc33ddeecac
出典メモuspto-grants-1999_02