참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 3-Fluorocatechol | HCID 67764 | — |
| 반응물 | Magnesium Chloride | HCID 5360315 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | tert-Butyl methyl ether | HCID 15413 | — |
| 생성물 | 4-Fluoro-2,3-dihydroxybenzaldehyde | HCID 45119103 | 19.6% |
반응 단계
Magnesium chloride (3.71 g, 33 mmol) was added portionwise at room temperature to a solution of 3-fluorocatechol (2 g, 15.6 mmol) in acetonitrile (20 mL), followed by triethylamine (13.4 mL, 97.5 mmol). Paraformaldehyde (3.16 g, 105.3 mmol) was then added to the stirred suspension and the mixture was heated at reflux for 5 hours. The mixture was cooled to room temperature then poured into a mixture of 5% HCl and TBME. The organic phase was separated, and the aqueous layer re-extracted with TBME. The combined organic extracts were washed with brine, dried over sodium sulphate and the solvent removed under reduced pressure. The crude mixture (˜1:1 starting material:product) was purified on normal silica in neat DCM followed by DCM/MeOH 96:4 and 90:10 to yield 478 mg of 28 still contaminated with 11.4% w/w of 3-fluorocatechol.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08198302B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-87e79cbc614f479d95cef12d52eb50aa |
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| 출처 메모 | uspto-grants-2012_06 |
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