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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272732생성일: 2026년 10월 26일

4-Methyl-5-(2-hydroxyethyl)thiazole → 5-[2-(4-Bromo-2-methoxyphenoxy)ethyl]-4-methyl-1,3-thiazole

https://huagongshe.com/reaction/272732

반응식

참여 물질

역할이름HCID투입량
반응물4-Methyl-5-(2-hydroxyethyl)thiazoleHCID 1136—
반응물TriphenylphosphineHCID 11776—
반응물4-Bromo-2-methoxyphenolHCID 262234—
반응물Dibenzyl azodicarboxylateHCID 5387121—
용매TetrahydrofuranHCID 8028—
생성물5-[2-(4-Bromo-2-methoxyphenoxy)ethyl]-4-methyl-1,3-thiazoleHCID 69217389—

반응 단계

A mixture of 4-bromo-2-methoxy-phenol (50.8 mg, 0.25 mmol), 2-(4-methyl-thiazol-5-yl)-ethanol (49.5 mg, 0.25 mmol) and polymer-supported triphenyl phosphine (250 mg, 0.75 mmol) in THF (2.5 mL) was stirred at room temperature for 20 minutes. DBAD (86.3 mg, 0.375 mmol) was added and the mixture was stirred overnight at room temperature. The reaction mixture was filtered through Celite®, rinsing with THF and methanol. The filtrate was concentrated, diluted with ethyl acetate, washed with water and brine, dried (MgSO4), filtered and concentrated. The concentrate was purified by column chromatography on silica gel (10 to 20% ethyl acetate in hexane) to give the title compound. MS (ESI) m/e 329 (M+H)+; 1H NMR (300 MHz, DMSO-d6) □ 8.82 (s, 1H), 7.12 (d, J=2.4 Hz, 1H), 7.03 (dd, J=8.5, 2.4 Hz, 1H), 6.91 (d, J=8.5 Hz, 1H), 4.10 (t, J=6.4 Hz, 2H), 3.77 (s, 3H), 3.20 (t, J=6.4 Hz, 2H), 2.35 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456169B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-ed514b5f95dd4b72bf78e549e5649397
출처 메모uspto-grants-2008_11