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HRID 21524作成日:2026年10月26日

Diazald → 1-Diazo-3-{o-[5-(2,4-dichlorophenoxy)-2-nitrophenoxy]phenoxy}-2-propanone

https://huagongshe.com/reaction/21524

反応式

関与物質

役割名称HCID仕込み量
反応物DiazaldHCID 6628—
反応物Potassium HydroxideHCID 14797—
反応物HCID 19932413HCID 19932413—
溶媒MethanolHCID 887—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物1-Diazo-3-{o-[5-(2,4-dichlorophenoxy)-2-nitrophenoxy]phenoxy}-2-propanoneHCID 54022969—

反応条件

温度42 °C

反応手順

A mixture of potassium hydroxide in methanol (20.0 mL of a 4M solution ) is heated to 42° C. and treated dropwise with a mixture of N-methyl-N-nitroso-p-toluenesulfonamide (4 g, 18.7 mmol) in ether (40 mL). The diazomethane is distilled over, condensed with a dry ice/acetone condenser and collected. The diazomethane/ether solution is stirred in an ice-bath, treated dropwise with a solution of {o-[5-(2,4-dichlorophenoxy)-2-nitrophenoxy]phenoxy}acetyl chloride (1.09 g, 2.32 mmol) in tetrahydrofuran, stirred for 30 minutes and concentrated in vacuo to give the title product as a yellow oil which is identified by NMR spectral analyses.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05424280
出典データセットuspto-grants-1995_06
ORD IDord-d1f6cb8854ac44ce91cca18716b94224
出典メモuspto-grants-1995_06