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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1057273생성일: 2026년 10월 26일

Ethyl Acetate → 7-Methyloxymethyloxy-4-trifluoromethylcoumarin

https://huagongshe.com/reaction/1057273

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Potassium CarbonateHCID 11430—
반응물Bromomethyl methyl etherHCID 83093—
반응물7-Hydroxy-4-trifluoromethylcoumarinHCID 5375667—
용매Diethyl EtherHCID 3283—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
용매HexaneHCID 8058—
생성물7-Methyloxymethyloxy-4-trifluoromethylcoumarinHCID 98603304%

반응 조건

온도2.5 °C

반응 단계

7-Methyloxymethyloxy-4-trifluorocoumarin (MOMFC) was prepared as follows: A mixture of 7-hydroxy-4-trifluoromethylcoumarin (230 mg, 1 mmol) and K2CO3 (248 mg, 1.5 mmol), in DMF (15 mL) was vigorously stiffed at 0-5° C. for 25 min. Bromomethyl methyl ether (0.97 mL, 10.0 mmol), was then added quickly to the reaction. The bright yellow mixture was stirred at 0-5° C. for 45 min during which time the reaction turned to a colorless solution. The reaction was allowed to continue to stir at 0-5° C. while monitoring by TLC (Rf=0.54, 1:1 EtOAc/:Hexane and Rf=0.24, CHCl3) and stopped at the time when product decomposition was detected. The reaction was then brought up in Et2O (35 mL), extracted with 30 mL of a saturated NaHCO3 solution. The aqueous layer was extracted two more times with Et2O (30 mL), the ether fractions were then combined, dried with anhydrous NaSO4, filtered and evaporated under reduced pressure. Chromatography of the crude product on silica gel (gradient 0-5% MeOH in CHCl3) gave 11 mg of the purified 7-methyloxymethyloxy-4-trifluoromethylcoumarin (MOMFC) as a white solid. 1H NMR (500 MHz, CDCl3): δ03.49 (s, 3H), 5.26 (s, 2H), 6.64 (s, 1H), 7.08-7.02 (m, 2H), 7.64 (d, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06514687B1
출처 데이터셋uspto-grants-2003_02
ORD IDord-a19f30f980eb4295b32bcfade89d2054
출처 메모uspto-grants-2003_02