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HRID 1434437作成日:2026年10月27日

(4-(Benzyloxy)phenyl)methanol → 4-Benzyloxybenzylamine

https://huagongshe.com/reaction/1434437

反応式

関与物質

役割名称HCID仕込み量
反応物(4-(Benzyloxy)phenyl)methanolHCID 70043—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物P,P-Diphenylphosphinic azideHCID 199401—
溶媒TolueneHCID 1140—
生成物4-BenzyloxybenzylamineHCID 429284581%

反応手順

To a solution of 4-benzyloxybenzyl alcohol (3.1 g) in toluene (40 ml) were sequentially added diphenylphosphoryl azide (4.8 g) and 1,8-diazabicyclo[5.4.0]undec-7-ene (2.6 g), and the solution was stirred for 25 hours at room temperature. The solution was extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. Obtained by purifying the residue by silica gel column chromatography (hexane-ethyl acetate system), to a solution of the resulting 1-azidomethyl-4-benzyloxybenzene (3.0 g) in tetrahydrofuran (40 ml) were sequentially added water (3 ml) and triethylphosphine (2.0 ml), and the solution was stirred for 1 hour and 10 minutes at room temperature. The reaction solution was concentrated in vacuo, extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by NH silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (2.5 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07612114B2
出典データセットuspto-grants-2009_11
ORD IDord-3b87955c2f6a45379aae11a6f8fa50f5
出典メモuspto-grants-2009_11