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HRID 1914687作成日:2026年10月26日

Morpholine → 4-(3-Methoxy-5-nitrobenzoyl)morpholine

https://huagongshe.com/reaction/1914687

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物3-Methoxy-5-nitrobenzoic acidHCID 5300212—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物4-(3-Methoxy-5-nitrobenzoyl)morpholineHCID 29908391—

反応手順

3-nitro-5-methoxybenzoic acid (900 mg; 4.57 mmol; 1 eq; commercially available IMPAMEX) is dissolved in THF (5 mL) at room temperature. 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.05 g; 5.48 mmol; 1.2 eq) and 1-hydroxybenzotriazole hydrate (987 mg; 7.3 mmol; 1.6 eq) are added in DCM (20 mL). The reaction mixture is stirred at room temperature for 25 min before adding morpholine (795.44 mg; 9.13 mmol; 2 eq). After 3 h, the reaction mixture is quenched with water and the organic phase recovered and washed with citric acid (5%). The aqueous phase is extracted with DCM. The organic phase is dried over MgSO4, and the solvent is evaporated under reduced pressure to afford 1.2 g (99%) as a yellow solid. The next step is carried out directly on the crude material. LC/MS: (ES+): 267.3; (ES−): 265.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08614215B2
出典データセットuspto-grants-2013_12
ORD IDord-5a083985db42425e964aad1247059a22
出典メモuspto-grants-2013_12