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HRID 882965作成日:2026年10月23日

1,2-Dichloroethane → (4-Bromo-3-fluorophenyl)(morpholin-4-yl)methanone

https://huagongshe.com/ja/reaction/882965

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物EthylmorpholineHCID 7525—
反応物MorpholineHCID 8083—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物4-Bromo-3-fluorobenzoic acidHCID 2773341—
溶媒DimethylformamideHCID 6228—
生成物(4-Bromo-3-fluorophenyl)(morpholin-4-yl)methanoneHCID 4847411598.5%

反応手順

A 500 mL flask was charged with 4-bromo-3-fluorobenzoic acid (5.00 g, 22.83 mmol), 100 mL DMF, morpholine (2.4 ml, 27.5 mmol), and 4-Ethylmorpholine (8.6 ml, 67.9 mmol). HOBt (4.32 g, 32.0 mmol) was added followed by EDC (5.25 g, 27.4 mmol) and the reaction allowed to stir at room temperature for 18 hours. The reaction was concentrated and the resulting orange syrup taken up in 100 mL EtOAc and 100 mL water. The organic layer was washed with 100 mL 2N HCl, 100 mL saturated sodium bicarbonate, and 100 mL saturated sodium chloride. The organic was then dried with MgSO4, filtered, and concentrated to give 6.476 g (98%) of a viscous yellow oil. This material was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08236799B2
出典データセットuspto-grants-2012_08
ORD IDord-77d51c2daee940da81507bf578f69cff
出典メモuspto-grants-2012_08