Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Formaldehyde → 2-Hydroxy-4-iodobenzaldehyde
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 3-Iodophenol | HCID 12272 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Magnesium Chloride | HCID 5360315 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2-Hydroxy-4-iodobenzaldehyde | HCID 18351513 | 160.1% |
반응 단계
To a solution of 3-iodophenol (3.00 g, 13.6 mmol) in acetonitrile (50 mL) was added magnesium chloride (3.89 g, 40.9 mmol), triethylamine (7.6 mL, 55 mmol), and paraformaldehyde (1.64 g, 55 mmol). The reaction mixture was refluxed overnight, then neutralized with saturated aqueous ammonium chloride. The resultant red precipitate was removed by filtration, and the filtrate was extracted with ethyl acetate. The precipitate was dissolved in methanol and added to the combined organic extracts, which were then dried over magnesium sulfate. The solvent was removed under reduced pressure to provide an orange solid (5.4 g) as the crude product. This material was used in the subsequent step without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07420066B2 |
| 출처 데이터셋 | uspto-grants-2008_09 |
| ORD ID | ord-02721cc0f01345be9e12390ff0c5239e |
| 출처 메모 | uspto-grants-2008_09 |