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HRID 2051969作成日:2026年10月25日

Ethyl Acetate → dibutyl 3-(N-benzyloxy-N-ethoxycarbonylamino)propylphosphonate

https://huagongshe.com/reaction/2051969

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物ethyl N-phenylmethoxycarbamateHCID 255288—
反応物Sodium ethoxideHCID 2723922—
反応物Dibutyl 3-chloropropylphosphonateHCID 20337237—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物dibutyl 3-(N-benzyloxy-N-ethoxycarbonylamino)propylphosphonateHCID 2033723042.8%

反応手順

A solution of ethyl N-benzyloxycarbamate (7.80 g.) in absolute ethanol (5 ml.) was added dropwise to a solution of sodium ethoxide in absolute ethanol [Na: 920 mg., absolute C2H5OH: 100 ml.] at 70° C. and the mixture was stirred at the same temperature for 30 minutes. To the mixture was added dropwise dibutyl 3-chloropropylphosphonate (10.8 g.), whereafter the reaction mixture was refluxed with stirring for 22 hours. The resultant mixture was cooled to give precipitates, which were filtered off. The filtrate was concentrated under reduced pressure to give a residue. To the residue was added ethyl acetate (100 ml.) and water (50 ml.). The ethyl acetate layer was separated, dried over magnesium sulfate and then concentrated under reduced pressure to give an oily residue (16.6 g.). The residue was subjected to column chromatography on silica gel with an eluent (chloroform). Fractions containing the object compound were collected and concentrated under reduced pressure to give oily dibutyl 3 -(N-benzyloxy-N-ethoxycarbonylamino)propylphosphonate (7.33 g.)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04182758
出典データセットuspto-grants-1980_01
ORD IDord-0e95dd514f3246018aadbc46dab0855e
出典メモuspto-grants-1980_01