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HRID 443862作成日:2026年10月27日

Diethyl Ether → Benzeneacetic acid, 4-chloro-alpha-(1-methylethyl)-

https://huagongshe.com/reaction/443862

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物TriethylammoniumHCID 1385867—
反応物2-(4-Chlorophenyl)-3-methylbutanoyl chlorideHCID 4178001—
生成物Benzeneacetic acid, 4-chloro-alpha-(1-methylethyl)-HCID 16197—

反応手順

A solution was prepared by admixing 3.0 grams (0.014 mole) of 6-(phenoxy)picolinalcohol, 3.5 grams (0.015 mole) of 2-isopropyl-2-(4-chlorophenyl)acetic acid chloride 10 milliliters of triethylammonium and 100 milliliters of dry ether. The reaction mixture was agitated at room temperature for 1 hour. The resulting reaction product mixture was successively washed with dilute hydrochloric acid, dilute sodium hydroxide, dried over anhydrous magnesium sulfate, filtered through silica gel and concentrated to give 5.3 grams of the desired 4-chloro-α-(1-methylethyl)benzeneacetic acid:(6-phenoxy-2-pyridinyl)methyl ester. The product, a viscous yellow oil, had a refractive index of 1.5664 and the structure of the product was confirmed by NMR. Upon analysis, the product was found to have carbon, hydrogen and nitrogen contents of 68.83, 5.19 and 3.10 percent, respectively, as compared with the theoretical contents of 69.78, 5.60 and 3.54 percent, respectively, as calculated for the above named compounds (Compound No. 2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04262001
出典データセットuspto-grants-1981_04
ORD IDord-f5828290e624466a9eb10152cffb7030
出典メモuspto-grants-1981_04