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HRID 2172005作成日:2026年10月25日

1-(Diphenylmethyl)azetidin-3-ol → 1-(Diphenylmethyl)-3-[(2-methylprop-2-en-1-yl)oxy]azetidine

https://huagongshe.com/reaction/2172005

反応式

関与物質

役割名称HCID仕込み量
反応物1-(Diphenylmethyl)azetidin-3-olHCID 330448—
反応物3-Bromo-2-methyl-1-propeneHCID 357785—
反応物Potassium tert-butoxideHCID 23665647—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Diphenylmethyl)-3-[(2-methylprop-2-en-1-yl)oxy]azetidineHCID 6715455494%

反応手順

A solution of 1-diphenylmethylazetidin-3-ol (239 mg, 1.0 mmol) in THF (3.6 mL) was cooled to 0° C. t-BuOK (1M in THF, 3.6 mL) was added dropwise and the reaction mixture was stirred at room temperature for 1 h then cooled to 0° C. 3-Bromo-2-methyl-1-propene (504 μL, 5.0 mmol) was added and the solution was stirred from 0° C. to room temperature overnight. The reaction mixture was diluted with H2O and extracted twice with EtOAc. The organic layers were combined, dried over Na2SO4 and concentrated to dryness to give the title compound (276 mg, 94%) as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09051321B2
出典データセットuspto-grants-2015_06
ORD IDord-a34738a2d6dc4e64941217b9a713a7ee
出典メモuspto-grants-2015_06