戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2421556作成日:2026年10月25日

Glycidyl benzoate → 2-Hydroxy-3-phenylcarbonyloxypropyl (2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoate

https://huagongshe.com/reaction/2421556

反応式

関与物質

役割名称HCID仕込み量
反応物Glycidyl benzoateHCID 25998—
反応物N-(tert-Buloxycarbonyl)-3,4-dihydroxy-L-phenylalanineHCID 14217229—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒TolueneHCID 1140—
生成物2-Hydroxy-3-phenylcarbonyloxypropyl (2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoateHCID 6020725226%

反応手順

A solution of oxiran-2-ylmethyl benzoate (3.0 g, 16.8 mmol), (2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoic acid (6.0 g, 20.2 mmol), and tetrabutylammonium bromide (542 mg, 1.7 mmol) in anhydrous toluene was heated to 90° C. for 18 hrs. The reaction mixture was concentrated to dryness under reduced pressure, diluted with ethyl acetate, and washed with water twice followed by the addition of a saturated NaHCO3 solution and brine. The organic layer was dried through MgSO4 and concentrated under reduced pressure. Chromatography (silica gel, 1:1 ethyl acetate/hexane) of the residue afforded 2.05 g (26%) of 2-Hydroxy-3-phenylcarbonyloxypropyl (2S)-3-(3,4-dihydroxyphenyl)-2-[(tert-butoxy)carbonylamino]propanoate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07956212B2
出典データセットuspto-grants-2011_06
ORD IDord-4f5a9d1cc9a74b45869df704ba6ea08e
出典メモuspto-grants-2011_06