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Tributylphosphine → 2-[2-(2,6-Dichloro-4-methylphenoxy)ethoxy]thiazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tributylphosphine | HCID 13831 | — |
| 反応物 | 2,6-Dichloro-4-methylphenol | HCID 17077 | — |
| 反応物 | 2-(Thiazol-2-yloxy)ethanol | HCID 45121950 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 2-[2-(2,6-Dichloro-4-methylphenoxy)ethoxy]thiazole | HCID 66783584 | 69% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08138340B2 |
| 出典データセット | uspto-grants-2012_03 |
| ORD ID | ord-bb51e01ccef1426a8f2a62160c0117c6 |
| 出典メモ | uspto-grants-2012_03 |