関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Dodecyne | HCID 69821 | — |
| 反応物 | 5-Bromo-2-hydroxybenzene-1,3-dicarbaldehyde | HCID 5260206 | — |
| 触媒 | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| 触媒 | HCID 178419050 | HCID 178419050 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 5-(Dodec-1-YN-1-YL)-2-hydroxybenzene-1,3-dicarbaldehyde | HCID 59710865 | 46% |
反応手順
2,6-Diformyl-4-bromophenol (2.50 g, 10.9 mmol), 1-dodecyne (2.00 g, 12.0 mmol), CuI (65 mg, 0.33 mmol), and bis(triphenylphosphine)palladium)II) dichloride were suspended in degassed acetonitrile (MeCN) (5 mL) and degassed benzene (1 mL). The yellow suspension was sparged with argon for 30 min and degassed Et3N (1 mL) was added. The resulting brown suspension was sealed in a pressure vial, warmed to 80° C. and held there for 12 h. The mixture was then partitioned between EtOAc and KHSO4 solution. The organic layer was separated, washed with brine, dried (MgSO4) and concentrated under reduced pressure. The dark yellow oil was purified by column chromatography on silica gel (25% Et2O in hexanes) to give 1.56 g (46%) of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07595368B2 |
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| 出典データセット | uspto-grants-2009_09 |
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| ORD ID | ord-81fc3fbce02449e0b0669b26f7226ded |
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| 出典メモ | uspto-grants-2009_09 |
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