Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tributylphosphine → 2-[2-(2,6-Dichloro-4-methylphenoxy)ethoxy]thiazole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tributylphosphine | HCID 13831 | — |
| 반응물 | 2,6-Dichloro-4-methylphenol | HCID 17077 | — |
| 반응물 | 2-(Thiazol-2-yloxy)ethanol | HCID 45121950 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2-[2-(2,6-Dichloro-4-methylphenoxy)ethoxy]thiazole | HCID 66783584 | 69% |
반응 단계
A mixture of 2-(thiazol-2-yloxy)ethanol (6.39 g, 44.0 mmol), 2,6-dichloro-p-cresol (15.6 g, 88.0 mmol), azodicarboxylic-dipiperidide (22.2 g, 88.0 mmol) and PBu3 (85%, 38.3 mL, 132 mmol) in toluene (325 mL) was heated to reflux for 30 min. The mixture was allowed to cool to rt, filtered, and the precipitate was washed thoroughly with toluene. The filtrate was evaporated under reduced pressure. The residue was diluted with EtOAc, and washed with aq. 1M NaOH (4×). The org. phase was dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the crude by FC (EtOAc/heptane 1:19→1:9→1:4) yielded the title compound as a colourless solid (9.24 g, 69%). LC-MS: tR=1.06 min, ES+: 304.05.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08138340B2 |
| 출처 데이터셋 | uspto-grants-2012_03 |
| ORD ID | ord-bb51e01ccef1426a8f2a62160c0117c6 |
| 출처 메모 | uspto-grants-2012_03 |