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HRID 351537作成日:2026年10月25日

Hydrochloric Acid → N-(4-n-pentyloxybenzoyl)-N,O-dimethylhydroxylamine

https://huagongshe.com/reaction/351537

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N,O-DimethylhydroxylamineHCID 14232—
反応物Oxalyl chlorideHCID 65578—
反応物Benzoic acid, 4-(pentyloxy)-HCID 85153—
反応物p-Pentoxybenzoyl chlorideHCID 94910—
溶媒PyridineHCID 1049—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物N-(4-n-pentyloxybenzoyl)-N,O-dimethylhydroxylamineHCID 22713252—

反応手順

To a suspension of 4-n-pentyloxybenzoic acid (5.0 g) in toluene was added oxalyl chloride (15 ml) and N,N-dimethylformamide (0.1 ml) and the mixture was stirred for 2 hours at room temperature. The solvents were evaporated under reduced pressure to give crude 4-n-pentyloxybenzoyl chloride. To a suspension of N,O-dimethylhydroxylamine a hydrochloride (3.51 g) and pyridine (5.82 ml) in tetrahydrofuran (25 ml) was added the solution of crude 4-n-pentyloxybenzoyl chloride in tetrahydrofuran (25 ml) dropwise at 0° C. and the mixture was stirred for 3 hours at room temperature. To the reaction mixture 1N HCl was added and extracted with ethyl acetate. The organic layer was separated, washed with water and brine, dried over magnesium sulfate and evaporated under reduced pressure to give N-(4-n-pentyloxybenzoyl)-N,O-dimethylhydroxylamine (4.63 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06743776B2
出典データセットuspto-grants-2004_06
ORD IDord-12a0b63b4cde4eee8a712bc2e9c58201
出典メモuspto-grants-2004_06