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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 363457생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfideHCID 1068—
반응물Sulfuric AcidHCID 1118—
반응물Sodium hydrideHCID 24758—
반응물1,3-CyclopentanedioneHCID 77466—
반응물3,4-epoxy-6-pentafluoroethyl-2,2-bisfluoromethyl-3,4-dihydro-2H-1-benzopyranHCID 15871792—
촉매copper(I) bromideHCID 24593—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물trans-6-pentafluoroethyl-2,2-bisfluoromethyl-3,4-dihydro-4-(3-oxo-cyclopent-1-enyloxy)-2H-1-benzopyran-3-olHCID 867506143.4%

반응 조건

온도-20 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05874446
출처 데이터셋uspto-grants-1999_02
ORD IDord-1fbfe959989745e5821f9fc33ddeecac
출처 메모uspto-grants-1999_02