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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Methyl-5-(2-hydroxyethyl)thiazole | HCID 1136 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | 4-Bromo-2-methoxyphenol | HCID 262234 | — |
| 반응물 | Dibenzyl azodicarboxylate | HCID 5387121 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-[2-(4-Bromo-2-methoxyphenoxy)ethyl]-4-methyl-1,3-thiazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07456169B2 |
|---|
| 출처 데이터셋 | uspto-grants-2008_11 |
|---|
| ORD ID | ord-ed514b5f95dd4b72bf78e549e5649397 |
|---|
| 출처 메모 | uspto-grants-2008_11 |
|---|