돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 988948생성일: 2026년 10월 25일

Ethyl Acetate → 7-Methyloxymethyloxy-4-trifluoromethylcoumarin

https://huagongshe.com/reaction/988948

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 stirred 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): δ 03.49 (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 번호US06638713B2
출처 데이터셋uspto-grants-2003_10
ORD IDord-fac734f74c064198b86402553a462cf6
출처 메모uspto-grants-2003_10