참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dibromomethane | HCID 3024 | — |
| 반응물 | Phosphorus oxide (P4O10) | HCID 14812 | — |
| 반응물 | 5-Bromo-3,4-dihydroxybenzaldehyde | HCID 85405 | — |
| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 7-Bromo-1,3-dioxaindane-5-carbaldehyde | HCID 2320243 | 76% |
반응 단계
To a stirred solution of 3-bromo-4,5-dihydroxybenzaldehyde (10.50 g, 48.38 mmol) in DMF (145 mL) was added anhydrous KF (14.02 g, 241.9 mmol, dried for 24 hours under high vacuum/P2O5). After 15 minutes CH2Br2 was added all at once and the resulting mixture heated to 100–105° C. for 4 hours. The mixture was evaporated under reduced pressure and the residue was taken up in ether and water. The layers were separated, the aqueous layer was washed with ether (3×). The combined ether layers were washed with water (2×), brine and dried over anhydrous magnesium sulfate. After filtration, the mixture was concentrated under reduced pressure to give 8.42 g of 3-bromo-4,5-methylenedioxybenzaldehyde (76%) as a brownish solid. 1H NMR (500 MHz; CDCl3): δ 6.16 (s, 2H); 7.26 (s, 1H); 7.55 (s, 1H); 9.77 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07153875B2 |
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| 출처 데이터셋 | uspto-grants-2006_12 |
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| ORD ID | ord-94d30a6f70cd4a49bf1025ca9da9fd1d |
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| 출처 메모 | uspto-grants-2006_12 |
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