참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Iodoxybenzoic acid | HCID 108794 | — |
| 반응물 | [2-(3-Fluoro-4-methoxy-phenyl)-cyclopropyl]-methanol | HCID 22347600 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 생성물 | 2-(3-Fluoro-4-methoxy-phenyl)-cyclopropanecarbaldehyde | HCID 20792250 | 89.8% |
반응 단계
After [2-(3-fluoro-4-methoxy-phenyl)-cyclopropyl]-methanol (0.30 g, 1.52 mmol) obtained in Step A was dissolved in DMSO (5 mL), 2-iodoxybenzoic acid (1.248 g, 4.58 mmol) was added thereto at 0° C., and the mixture was stirred at room temperature for 3 hours. After the termination of the reaction, the reactant was concentrated under reduced pressure, added with water, and then extracted with EtOAc. The organic layer was separated, dried with MgSO4, concentrated under reduced pressure, and then purified by column chromatography (eluent, EtOAc/Hex=1/3) to obtain the title compound (0.265 g, 89%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09447044B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-11927d140f08417fa37a449300c73eae |
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| 출처 메모 | uspto-grants-2016_09 |
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