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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 624230생성일: 2026년 10월 26일

Hydrochloric Acid → 4-(2-Benzylthiazol-4-yl)aniline

https://huagongshe.com/reaction/624230

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물Ammonium HydroxideHCID 14923—
반응물2-Bromo-4'-nitroacetophenoneHCID 66840—
반응물2-PhenylethanethioamideHCID 731368—
촉매IronHCID 23925—
용매EthanolHCID 702—
생성물4-(2-Benzylthiazol-4-yl)anilineHCID 12463536—

반응 조건

온도140 °C

반응 단계

2-Bromo-1-(4-nitrophenyl)ethanone (0.5 g, 2.049 mmol) and 2-phenylethanethioamide (0.310 g, 2.049 mmol) were combined in ethanol (10 ml) in a 20 mL microwave reaction vessel and heated at 140° C. for 15 minutes. The solution was transferred to a 250 mL round bottom flask where it immediately solidified. The material was diluted with an additional ethanol (10 ml) and was heated at reflux with stirring until the solids were dissolved. Water (5.0 ml, 278 mmol), and hydrochloric acid (1 ml, 12.00 mmol) were added. Iron (0.625 g, 11.19 mmol) was added and the mixture was heated at reflux for 2 hours. The mixture was allowed to cool and 5 mL NH4OH was added. The material was filtered through a pad of diatomaceous earth and the pad was washed with 50 mL of ethyl acetate. The filtrate was washed with 100 mL of water and the aqueous phase was extracted with an additional 50 mL of ethyl acetate. The combined organic fractions were dried over sodium sulfate, filtered, and the solvent was removed under reduced pressure. The material was re-dissolved in 50 mL of ethyl acetate and filtered through a ¼-inch pad of silica gel. The pad was washed with an additional 50 mL of ethyl acetate and the combined filtrate was concentrated to provide the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09302989B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-3f4ebb7ed1c14c9792b833efd0771e13
출처 메모uspto-grants-2016_04