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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2402520생성일: 2026년 10월 26일

2,6-Dimethylaniline → 4-Amino-N-(2,6-dimethylphenyl)phthalimide

https://huagongshe.com/reaction/2402520

반응식

참여 물질

역할이름HCID투입량
반응물2,6-DimethylanilineHCID 6896—
반응물Sodium HydroxideHCID 14798—
반응물Stannous ChlorideHCID 24479—
반응물4-Nitrophthalic acid anhydrideHCID 230976—
용매Acetic AcidHCID 176—
용매Ethyl AcetateHCID 8857—
생성물4-Amino-N-(2,6-dimethylphenyl)phthalimideHCID 12403167.2%

반응 조건

온도100 °C

반응 단계

A mixture of 5-nitrophthalic anhydride (1.0 g, 5.2 mmol) and 2,6-dimethylaniline (0.65 mL, 5.3 mmol) in acetic acid (50 mL) was heated at 100° C. overnight (14 h). The reaction mixture was cooled, diluted with ethyl acetate and washed with saturated sodium bicarbonate. The organic phase was dried over anhydrous sodium sulfate, filtered and concentrated. The product was dissolved in ethanol (50 mL), tin (II) chloride (1.4 g, 6.2 mmol) was added and the mixture was heated to reflux for 5 h. The reaction mixture was cooled and made basic by adding aqueous 2 N sodium hydroxide. Ethyl acetate was added and the layers were separated. The organic layer was washed with water and saturated sodium chloride, dried over anhydrous sodium sulfate, filtered and concentrated on a rotary evaporator to give 5-amino-2-(2,6-dimethylphenyl)isoindoline-1,3-dione (0.93 g, 67%), which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08796294B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-cf9aaa88b74e4573b5c46299e5a1e6ea
출처 메모uspto-grants-2014_08