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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2987생성일: 2026년 10월 24일

Acetone → 2-(4-Acetamidophenoxy)-2-methylpropanoic acid

https://huagongshe.com/ko/reaction/2987

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물AcetaminophenHCID 1983—
반응물ChloroformHCID 6212—
반응물Sodium HydroxideHCID 14798—
반응물2-(4-Aminophenoxy)-2-methylpropanoic acidHCID 2774958—
생성물2-(4-Acetamidophenoxy)-2-methylpropanoic acidHCID 1487985560%

반응 단계

FIG. 2A illustrates a reaction scheme for preparing 2-(4-aminophenoxy)-2-methyl propionic acid, a compound that is useful as a precursor in the preparation of Group I compounds. In accordance with the scheme of FIG. 2A, 8 grams (g) (0.2 mol) of pulverized sodium hydroxide is added to a suspension of 5.28 g (0.035 mol) of p-acetamidophenol in 23 ml (0.4 mol) of acetone. The reaction mixture is stirred at room temperature for 1/2 hour. Subsequently, 3.58 g (0.03 mol) of chloroform is added dropwise over the course of 30 minutes. The reaction mixture is stirred overnight at room temperature and acetone is removed under vacuum. The residue is dissolved in water (10 ml), followed by acidification with 37% hydrochloric acid (HCl) to produce a pale yellow precipitate of 2-(4-acetaminophenoxy)-2-methyl propionic acid (5 g, 60% yield), crystallized from methanol, mp 69°-71° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731454
출처 데이터셋uspto-grants-1998_03
ORD IDord-8d4bf2d31e824543ac5f1049cd6477c4
출처 메모uspto-grants-1998_03