돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272697생성일: 2026년 10월 26일

4-Methyl-5-(2-hydroxyethyl)thiazole → 4-[2-(4-Methyl-1,3-thiazol-5-yl)ethoxy]-2-nitroaniline

https://huagongshe.com/reaction/272697

반응식

참여 물질

역할이름HCID투입량
반응물4-Methyl-5-(2-hydroxyethyl)thiazoleHCID 1136—
반응물TriphenylphosphineHCID 11776—
반응물Di-tert-butyl azodicarboxylateHCID 97268—
반응물4-Amino-3-NitrophenolHCID 3758882—
용매TetrahydrofuranHCID 8028—
생성물4-[2-(4-Methyl-1,3-thiazol-5-yl)ethoxy]-2-nitroanilineHCID 6921998386.2%

반응 단계

A mixture of 4-amino-3-nitrophenol (386 mg, 2.5 mmol), 2-(4-methyl-1,3-thiazol-5-yl)ethanol (0.299 mL, 2.5 mmol), polymer supported triphenylphosphine (1.25 g, 3 mmol/g, 3.75 mmol), and di-tert-butyl azodicarboxylate (864 mg, 3.75 mmol) in THF (10 mL) was stirred at room temperature for 16 hours. Filtered through Celite and concentrated under vacuum. The residue was purified by flash column chromatography on silica gel with 1:1 hexanes/ethyl acetate to provide 602 mg (86%) of the desired product. MS (DCI) m/e 279 (M+H)+, 1H NMR (300 MHz, DMSO-d6): □ 8.83 (s, 1H), 7.37 (d, J=3.05 Hz, 1H), 7.25 (s, 2H), 7.16 (dd, J=8.99, 2.88 Hz, 1H), 7.01 (s, 1H), 4.10 (t, J=6.27 Hz, 2H), 3.19 (t, J=6.27 Hz, 2H), 2.35 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456169B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-409df72e33cf45d8a976a3b4eefceee5
출처 메모uspto-grants-2008_11