참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Naphthoic acid | HCID 6847 | — |
| 반응물 | 4-Fluorophenol | HCID 9732 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | 2-Bromo-4-tert-butylbenzoic acid | HCID 236352 | — |
| 촉매 | Benzene;bis(copper(1+));bis(trifluoromethanesulfonate) | HCID 2734754 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-(4-Fluorophenoxy)-4-tert-butylbenzoic acid | HCID 58988089 | 39% |
반응 단계
A stirred suspension of 4-tert-butyl-2-bromobenzoic acid (0.26 g, 1.0 mmol), 4-fluoro phenol (0.22 g, 2.0 mmol), cesium carbonate (0.65 g, 2.0 mmol), copper trifluoromethanesulfonate-benzene complex (13 mg, 25 μmol), 1-naphthoic acid (0.34 g, 2.0 mmol), and 4 Å molecular sieves (0.25 g) in toluene (10 mL) and EtOAc (5 μL) was heated at 110° C. for 16 h. The reaction was concentrated under reduced pressure and purified by silica gel chromatography (0%-5% MeOH—CH2Cl2) to afford 2-(4-fluorophenoxy)-4-tert-butylbenzoic acid (0.11 g, 39% yield) as a white solid. LC/MS: m/z 289.0 (M+H)+ at 3.58 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)). 1H NMR (400 MHz, CDCl3) δ 8.12 (d, J=8.3 Hz, 1H), 7.24 (d, J=1.7 Hz, 1H), 7.14-7.05 (m, 4H), 6.84 (d, J=1.6 Hz, 1H), 1.23 (s, 9H) ppm.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08841483B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-ae47c4adfc9d403c835af054aab39927 |
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| 출처 메모 | uspto-grants-2014_09 |
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