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HRID 215718作成日:2026年10月25日

Hydrochloric Acid → 3-(2-Methoxy-3-methylthio-4-(trifluoromethyl)benzoyloxy)-cyclohex-2-enone

https://huagongshe.com/reaction/215718

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TriethylamineHCID 8471—
反応物1,3-CyclohexanedioneHCID 10434—
反応物Oxalyl chlorideHCID 65578—
反応物2-Methoxy-3-methylthio-4-(trifluoromethyl)benzoic acidHCID 66957907—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物3-(2-Methoxy-3-methylthio-4-(trifluoromethyl)benzoyloxy)-cyclohex-2-enoneHCID 6695790647%

反応手順

133 mg (1.05 mmol) of oxalyl dichloride and three drops of N,N-dimethylformamide were added in succession to 200 mg (purity 78% by weight, 0.59 mmol) of 2-methoxy-3-methylthio-4-(trifluoromethyl)benzoic acid in 20 ml of dichloromethane. After the elimination of gas had ceased, the mixture was heated under reflux for another 10 min. The content was then cooled to RT and freed from the solvent. 93 mg (0.83 mmol) of 1,3-cyclohexanedione were added to the residue in 20 ml of dry dichloromethane, and 152 mg (1.50 mmol) of triethylamine were then added dropwise. The mixture was stirred at RT for 16 h. For work-up, 3 ml of 1M hydrochloric acid were added to the contents. After phase separation, the organic phase was freed from the solvent. The residue was purified chromatographically, which isolated 100 mg of 3-(2-methoxy-3-methylthio-4-(trifluoromethyl)benzoyloxy)-cyclohex-2-enone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193121B2
出典データセットuspto-grants-2012_06
ORD IDord-4070c308f2f64353b9bdaddc1bc4a3d9
出典メモuspto-grants-2012_06