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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131949생성일: 2026년 10월 23일

2-Aminothiazole → 3-(2-Methyl-allyloxy)-4-nitrotoluene

https://huagongshe.com/ko/reaction/131949

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물Methallyl alcoholHCID 10557—
반응물Benzene, 2-fluoro-4-methyl-1-nitro-HCID 67966—
반응물4-Methyl-2-[(2-methylprop-2-en-1-yl)oxy]anilineHCID 45091245—
생성물HCID 59733018HCID 5973301870%
생성물3-(2-Methyl-allyloxy)-4-nitrotolueneHCID 6035784475%

반응 단계

3-(2-Methyl-allyloxy)-4-nitrotoluene (0.78 g, 75%) was prepared from methallyl alcohol and 3-fluoro-4-nitrotoluene (0.77 g, 5.0 mmol) following the general procedure G. This was reduced to 4-methyl-2-(2-methyl-allyfoxy)aniline (0.47 g, 70%) following general procedure B. 1-[4-Methyl-2-(2-methyl-allyloxy)-phenyl]-3-thiazol-2-yl-urea (210 mg, 70%) was prepared from 4-methyl-2-(2-methyl-allyloxy)aniline (179 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384967B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-25995062b3c74c8cb170a8f08ba7950e
출처 메모uspto-grants-2008_06