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HRID 25280생성일: 2026년 10월 23일

Potassium Carbonate → (2-Ethoxymethoxy-5-(4-trifluoromethylphenyl)phenyl] 2,2,2-trifluoroethyl sulfide

https://huagongshe.com/ko/reaction/25280

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1,1,1-Trifluoro-2-iodoethaneHCID 67709—
반응물1,1'-Thiodi-[2-ethoxymethoxy-5-(4-trifluoromethylphenyl)benzene]HCID 22170890—
반응물Sodium Formaldehyde SulfoxylateHCID 23689980—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물(2-Ethoxymethoxy-5-(4-trifluoromethylphenyl)phenyl] 2,2,2-trifluoroethyl sulfideHCID 86587598151.1%

반응 단계

3.3 g (5.0 mmol) of 1,1′-thiodi-[2-ethoxymethoxy-5-(4-trifluoromethylphenyl)benzene], 3.0 g (19.5 mmol) of Rongalite, 3.0 g (21.7 mmol) of potassium carbonate and 3.2 g (17.6 mmol) of 2,2,2-trifluoroethyl iodide were stirred in 50 ml of N,N-dimethylformamide at room temperature for 3 hours. The resulting reaction mixture was poured into 300 ml of water and extracted with 50 ml of ethyl acetate twice. The ethyl acetate layer was washed with 50 ml of water twice and dried over anhydrous magnesium sulfate, and the ethyl acetate was distilled off under reduced pressure. Purification of the residue by silica gel column chromatography afforded 3.1 g of (2-ethoxymethoxy-5-(4-trifluoromethylphenyl)phenyl] 2,2,2-trifluoroethyl sulfide (yield 75.6%) as a pale yellow viscous liquid (nD20 1.5213).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858639B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-c3157614ddee40f7b889ddcb92241301
출처 메모uspto-grants-2005_02