참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-(3,4-Dichlorophenoxy)-5-fluorobenzaldehyde | HCID 22019271 | — |
| 반응물 | Jones' reagent | HCID 131709961 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 2-(3,4-Dichlorophenoxy)-5-fluoro-benzoic acid | HCID 22019277 | — |
반응 단계
Alternatively, a solution of 4.28 g (15 mmol) of 2-(3,4-dichloro-phenoxy)-5-fluorobenzaldehyde (Preparation no. 5) in 25 mL of acetone was cooled to 5-10° C. and treated via syringe with 5.8 mL (15.6 mmol) of 2.67 M Jones reagent*. After 1 hr at this temperature, the reaction was quenched with 8 mL of isopropanol, allowed to warm to 25° C., and filtered through a pad of d.e. The filtrate was concentrated in vacuo to approximately ¼ volume, diluted with water and extracted several times with CHCl3. The organic layers were washed with water, then with saturated NaCl and finally dried over MgSO4 and concentrated to provide 2-(3,4-dichlorophenoxy)-5-fluoro-benzoic acid as a tan solid, 4.19 g. 1H-nmr (CDCl3, 400 MHz, δ): 7.78 (dd, 1H), 7.38 (d, 1H), 7.27 (m, 1H), 6.98 (m, 2H), 6.81 (dd, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06677378B2 |
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| 출처 데이터셋 | uspto-grants-2004_01 |
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| ORD ID | ord-f72ff8a8272c46549f0fb40dbe2dd129 |
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| 출처 메모 | uspto-grants-2004_01 |
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