참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfoxide | HCID 679 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | 2,5-Difluorobenzaldehyde | HCID 137663 | — |
| 반응물 | Dilithium Sulfide | HCID 10290727 | — |
| 생성물 | 3-Fluorobenzene-1,2-dicarbaldehyde | HCID 22325230 | 59% |
반응 단계
To a stirred solution of 17.5 g (123 mmol) of 2,5-difluorobenzaldehyde (Aldrich) in 615 mL of DMSO at ambient temperature was added 6.2 g (135 mmol) of lithium sulfide (Aldrich). The dark red solution was stirred at 75 C for 1.5 hours, or until the starting material was completely consumed, and then 34 g (135 mmol) of dibutyl mesylate aldehyde was added at about 50 C. The reaction mixture was stirred at 75 C for three hours or until the reaction was completed. The cooled solution was poured into water and extracted with ethyl acetate. The combined extracts were washed with water several times, dried (MgSO4) and concentrated in vacuo. Silica gel chromatographic purification of the crude product gave 23.6 g (59%) of fluorobenzene dialdehyde as a yellow oil: 1H NMR (CDCl3) d 0.87 (t, J=7.05 Hz, 6H), 1.0-1.4 (m, 8H), 1.5-1.78 (m, 4H), 3.09 (s, 2H), 7.2-7.35 (m, 1H), 7.5-7.6 (m, 2H), 9.43 (s, 1H) 10.50 (d, J=2.62 Hz, 1H)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06943189B2 |
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| 출처 데이터셋 | uspto-grants-2005_09 |
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| ORD ID | ord-19c0894312d14027be594246d09d1d8d |
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| 출처 메모 | uspto-grants-2005_09 |
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