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HRID 383482作成日:2026年10月26日

Triethylamine → 2,2-Dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonate

https://huagongshe.com/reaction/383482

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Trifluoromethanesulfonic anhydrideHCID 67749—
反応物4-Hydroxy-5,5-dimethyl-2(5H)-furanoneHCID 54720139—
溶媒DichloromethaneHCID 6344—
生成物2,2-Dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonateHCID 5892634889%

反応条件

温度-78 °C

反応手順

To a −78° C. stirred solution of 4-hydroxy-5,5-dimethyl-5H-furan-2-one (250 mg, 1.95 mmol) in 18 mL of anhydrous CH2Cl2, was added triethylamine (0.40 mL, 2.9 mmol) and Tf2O (0.49 mL, 2.9 mmol). The reaction was stirred at −78° C. for 30 minutes, and quenched with saturated NH4Cl solution (10 mL). The mixture was warmed up to room temperature and separated. The aqueous layer was extracted with CH2Cl2 (2×20 mL). All organic layers were combined, dried over Na2SO4 and evaporated to brown oil, which was purified by plugging through a short pad of silica gel column with EtOAc/hexanes (1/3). Evaporation of solvents gave 2,2-dimethyl-5-oxo-2,5-dihydrofuran-3-yl trifluoromethanesulfonate as a light brown oil (450 mg, 89%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367664B2
出典データセットuspto-grants-2013_02
ORD IDord-5991e68c395a48ea8b9586856d436e16
出典メモuspto-grants-2013_02