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HRID 219004作成日:2026年10月25日

Phosphate → (5R)-3-(6-bromohexyl)-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/219004

反応式

関与物質

役割名称HCID仕込み量
反応物PhosphateHCID 1061—
反応物1,6-DibromohexaneHCID 12368—
反応物Sodium hydrideHCID 24758—
反応物(5R)-5-(2,2-Dimethyl-4H-1,3-benzodioxin-6-yl)-1,3-oxazolidin-2-oneHCID 10933894—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物(5R)-3-(6-bromohexyl)-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-1,3-oxazolidin-2-oneHCID 66845427—

反応手順

A solution of (5R)-5-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-1,3-oxazolidin-2-one (5.00 g) and 1,6-dibromohexane (9.26 ml) in DMF (50 ml) at 0° under nitrogen was treated in three equal portions with sodium hydride (60% dispersion in mineral oil, 963 mg). The mixture was stirred at 0° for 30 min and then at 20° for a further 2.5 h. Phosphate buffer solution (pH 6.5, 50 ml) and water (150 ml) were added and the mixture was extracted with diethyl ether (2×150 ml). The combined extracts were washed with water (2×150 ml) and were dried (Na2SO4). The solvent was evaporated in vacuo and the residue was purified by flash chromatography on silica gel. Elution with MeOH-dichloromethane (1:4) gave the title compound (7.10 g). LCMS RT=3.52 min, ES+ve 412 (MH)+, 414 (MH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198483B2
出典データセットuspto-grants-2012_06
ORD IDord-0b19dcc3b7f24da59f1588d7e5d1c984
出典メモuspto-grants-2012_06