참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Chloroethanol | HCID 34 | — |
| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Methylparaben | HCID 7456 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | 1-Chloroethan-1-ol | HCID 12639035 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Benzoic acid, 4-(2-hydroxyethoxy)-, methyl ester | HCID 76670 | 44% |
반응 단계
Methyl 4-hydroxybenzoate (1.52 g, 10 mmol), 2-chloroethanol (960 mg, 12 mmol), potassium iodide (100 mg, 0.6 mmol) and cesium carbonate (4.56 g, 14 mmol) are combined with dry THF (50 mL) and the reaction mixture is stirred under reflux for 24 h. Additional chloroethanol (960 mg), cesium carbonate (4.56 g) and potassium iodide (100 mg) are added to the mixture and stirred under reflux for 24 h. The reaction mixture is cooled to room temperature and water and CH2Cl2 are added. The separated CH2Cl2 layer is dried over Na2SO4, filtered and evaporated. The crude product is purified using silica-gel column chromatography (hexane:EtOAc=3:1) to give the titled compound (862 mg, 44%). NMR (CDCl3): δ 8.02 (d, 2H, J=9.0 Hz), 6.97 (d, 2H, J=9.0 Hz), 4.17 (t, 2H, J=5.0 Hz), 4.03 (m, 2H), 3.92 (s, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07951826B2 |
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| 출처 데이터셋 | uspto-grants-2011_05 |
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| ORD ID | ord-e045882a519d42a8a6f9798cb93f57b3 |
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| 출처 메모 | uspto-grants-2011_05 |
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