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HRID 719070作成日:2026年10月27日

Ethyl Acetate → 7-Methyloxymethyloxy-4-trifluoromethylcoumarin

https://huagongshe.com/reaction/719070

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
反応物Bromomethyl methyl etherHCID 83093—
反応物7-Hydroxy-4-trifluoromethylcoumarinHCID 5375667—
溶媒Diethyl EtherHCID 3283—
溶媒ChloroformHCID 6212—
溶媒DimethylformamideHCID 6228—
溶媒HexaneHCID 8058—
生成物7-Methyloxymethyloxy-4-trifluoromethylcoumarinHCID 98603304%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07132252B2
出典データセットuspto-grants-2006_11
ORD IDord-eaf576a2db844e1cb2b6d3e908069146
出典メモuspto-grants-2006_11