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HRID 895714作成日:2026年10月23日

2-Methyl-2-butene → 5'-Nitro-2'-(6-cyano-2-naphthyloxy)-1,1'-biphenyl-2-carboxylic acid

https://huagongshe.com/ja/reaction/895714

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methyl-2-buteneHCID 10553—
反応物Sodium ChlorateHCID 516902—
反応物Hydrate;hydrochlorideHCID 21885828—
反応物4-(6-Cyano-2-naphthyloxy)-3-(2-formylphenyl)nitrobenzeneHCID 22380967—
反応物Sodium Phosphate, Monobasic, DihydrateHCID 23673460—
溶媒Acetonitrile--water (1/1)HCID 18373917—
生成物5'-Nitro-2'-(6-cyano-2-naphthyloxy)-1,1'-biphenyl-2-carboxylic acidHCID 22380897—

反応手順

The compound (4-(6-cyano-2-naphthyloxy)-3-(2-formylphenyl)nitrobenzene) (800 mg) obtained in a previous production example, 2-methyl-2-butene (1.4 ml) and sodium dihydrogen phosphate dihydrate (2 g) were dissolved in acetonitrile:water (2:1, 50 ml) and then sodium chlorate (1 g) was added. After reaction for one hour at room temperature, 1 N hydrochloric acid water was added and extraction was performed with ethyl acetate. The ethyl acetate layer was washed with 1N hydrochloric acid water and saturated saline and then dried over magnesium sulfate, and the solvent was distilled off to obtain 5′-nitro-2′-(6-cyano-2-naphthyloxy)-1,1′-biphenyl-2-carboxylic acid (800 mg). This was dissolved in toluene without purification and subjected to the same process as in Production Example 1 to obtain t-butyl 2′-(6-cyano-2-naphthyloxy)-5′-nitro-1,1′-biphenyl-2-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06916837B2
出典データセットuspto-grants-2005_07
ORD IDord-cd966038481b468884d58abc9f497da2
出典メモuspto-grants-2005_07