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HRID 2112017作成日:2026年10月27日

Monobenzone → Methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoate

https://huagongshe.com/reaction/2112017

反応式

関与物質

役割名称HCID仕込み量
反応物MonobenzoneHCID 7638—
反応物CyanomethylenetributylphosphoraneHCID 4622928—
反応物Methyl 2-((4-(3-hydroxypropyl)phenoxy)methyl)benzoateHCID 10780567—
溶媒TolueneHCID 1140—
生成物Methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoateHCID 6886971764.3%

反応手順

Methyl 2-{[4-(3-hydroxypropyl)phenoxy]methyl}benzoate (0.50 g, 1.66 mmol) and 4-(benzyloxy)phenol (0.33 g, 1.66 mmol) was added to a dry round bottomed flask fitted with a septum Dry toluene (10 ml) was added and N2 was flushed through the mixture for 5 minutes. (Tributylphosphoranylidene)acetonitrile (0.80 g, 3.33 mmol) was added dropwise and the reaction was performed in a single node microwave oven. After removing the solvent by evaporation the crude was purified by preparative HPLC (started with acetonitrile/buffer 60/40 and then the acetonitrile concentration was increased to 100%, the buffer was a mixture of acetonitrile/water 10/90 and ammonium acetate (0.1 M, column KR-100-7-C8, 50 mm×250 mm, flow 40 ml/min)). The product containing fractions were pooled and the acetonitrile was removed by evaporation. EtOAc (10 ml) was added and the organic phase was washed with two portions of brine and dried (MgSO4). Removing the solvent by evaporation gave 0.515 gram of methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]-propyl}phenoxy)methyl]benzoate (yield 64.1%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07521461B2
出典データセットuspto-grants-2009_04
ORD IDord-368ce849ae60442aba721e0c86c78c50
出典メモuspto-grants-2009_04