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HRID 4115作成日:2026年10月23日

Trifluoroacetic acid → (2S-trans)-(3-Amino-2-methyl-4-oxo-1-azetidinyl)phosphonic acid, 2-(3,4-dihydroxyphenyl)-2-oxoethyl ester, trifluoroacetate salt

https://huagongshe.com/ja/reaction/4115

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物AnisoleHCID 7519—
反応物PotassiumHCID 5462222—
反応物(2S-trans)-[1-[[2-(3,4-dihydroxyphenyl)-2-oxoethoxy]hydroxyphosphinyl]-2-methyl-4-oxo-3-azetidinyl]carbamic acid, 1,1-dimethylethyl esterHCID 131715446—
溶媒TolueneHCID 1140—
溶媒DichloromethaneHCID 6344—
生成物(2S-trans)-(3-Amino-2-methyl-4-oxo-1-azetidinyl)phosphonic acid, 2-(3,4-dihydroxyphenyl)-2-oxoethyl ester, trifluoroacetate saltHCID 131715444—

反応条件

温度0 °C

反応手順

To a suspension of (2S-trans)-[1-[[2-(3,4-dihydroxyphenyl)-2-oxoethoxy]hydroxyphosphinyl]-2-methyl-4-oxo-3-azetidinyl]carbamic acid, 1,1-dimethylethyl ester, monopotassium salt (117 mg, 0.25 mmol) in 2.5 ml of dry dichloromethane was added 100 μl of anisole and the mixture was then cooled to 0° C. in an ice bath under argon. Trifluoroacetic acid (1 ml) was added and the mixture stirred for two hours. The reaction mixture was diluted with 5 ml of dry toluene and the solvents removed in vacuo at room temperature yielding a yellow oily residue. The residue was triturated with hexanes (2×10 ml) followed by trituration with ether (2×10 ml). The solid was dried in vacuo yielding the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04723002
出典データセットuspto-grants-1988_02
ORD IDord-7b463b2c4b634287ae0797a585b376de
出典メモuspto-grants-1988_02