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HRID 1070060作成日:2026年10月27日

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

https://huagongshe.com/reaction/1070060

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US06251926B1
出典データセットuspto-grants-2001_06
ORD IDord-9cd42e1797b740298216b5ddeb00115d
出典メモuspto-grants-2001_06