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HRID 584376作成日:2026年10月25日

Tetrahydrofuran → 3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine

https://huagongshe.com/reaction/584376

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Potassium CarbonateHCID 11430—
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物N-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]phthalimideHCID 11732904—
溶媒EthanolHCID 702—
生成物3-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamineHCID 1092494697%

反応手順

Hydrazine monohydrate (0.661 ml) was added to a solution of N-[3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxy]phthalimide (3.00 g) in ethanol (25 ml)-tetrahydrofuran (25 ml) and heated under reflux for 3 hours. The reaction mixture was cooled to room temperature, an aqueous solution of potassium carbonate was added and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The remaining crystals were recrystallized from ethyl acetate-hexane to obtain 3-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyamine (2.04 g, yield 97%) as pale-yellow crystals. m.p. 81-82° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06924300B2
出典データセットuspto-grants-2005_08
ORD IDord-19bb44f0e0bc42d489cce83aafd9b25d
出典メモuspto-grants-2005_08