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HRID 1466736作成日:2026年10月27日

Methanesulfonic Acid → Dimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonate

https://huagongshe.com/reaction/1466736

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物Phthalaldehydic acidHCID 8406—
反応物Dimethyl ester phosphorous acidHCID 94853—
反応物SodiumHCID 5360545—
溶媒MethanolHCID 887—
生成物Dimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonateHCID 1111821367.3%

反応手順

To dry methanol (40 ml) was slowly added sodium (1.15 g, 50 mmol) at 0 under N2 atmosphere while stirring, then added dimethyl hydrogen phosphite (5.5 g, 50 mmol), and 2-formylbenzoic acid (5.25 g, 35 mmol). The ice bath was removed and the reaction mixture was stirred for 30 min at room temperature, and then the reaction mixture was slowly added methanesulfonic acid (5.5 g, 55 mmol) and concentrated at reduced pressure to give the crude residue. The crude residue was partitioned between DCM and cold water (100 ml each), and the organic phase was washed with water and brine, dried over sodium sulphate, filtered, and concentrated to give the crude product (5.7 g, 67%) as an off white solid, used in next step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08999985B2
出典データセットuspto-grants-2015_04
ORD IDord-a3ab18e4471645d0a8bbf30424b95826
出典メモuspto-grants-2015_04