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Pentane, 3-(bromomethyl)- → Dimethyl 5-(2-ethylbutoxyl)isophthalate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pentane, 3-(bromomethyl)- | HCID 77432 | — |
| 反応物 | 1,3-Benzenedicarboxylic acid, 5-hydroxy-, 1,3-dimethyl ester | HCID 83065 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | Dimethyl 5-(2-ethylbutoxyl)isophthalate | HCID 117704493 | — |
反応手順
Dimethyl 5-hydroxyisophthalate (0.44 g, 2.10 mmol) cesium carbonate (1.37 g, 4.20 mmol) and CH3CN (20 mL) were added to a round-bottom flask and stirred for 15-30 min. 3-(Bromomethyl)pentane (0.42 g, 2.52 mmol) was added and the reaction was stirred for 16 h. The solvent was removed under reduced pressure and the reaction mixture was partitioned between EtOAc (50 mL) and H2O (50 mL). The layers were separated and the aqueous layer was extracted with EtOAc (50 mL). The combined organics were dried over Na2SO4, filtered, and concentrated under reduced pressure to afford the desired product which was used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09439433B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-70fc3e9a7f11415ca319a2dbe0c30442 |
| 出典メモ | uspto-grants-2016_09 |