Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238625생성일: 2026년 10월 26일
(4-Benzyloxy-6-fluoro-3-methyl-naphthalen-2-yl)-methanol → 4-Benzyloxy-6-fluoro-3-methyl-naphthalene-2-carbaldehyde
https://huagongshe.com/reaction/238625
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (4-Benzyloxy-6-fluoro-3-methyl-naphthalen-2-yl)-methanol | HCID 59326595 | — |
| 반응물 | HCID 178418287 | HCID 178418287 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-Benzyloxy-6-fluoro-3-methyl-naphthalene-2-carbaldehyde | HCID 59326529 | 93.4% |
반응 단계
To a solution of (4-benzyloxy-6-fluoro-3-methyl-naphthalen-2-yl)-methanol (180 mg, 0.6 mmol) in dichloromethane (10 mL) was added pyridinium chlorochromate (260 mg, 1.2 mmol) in portions. After being stirred at room temperature for 3 hours, the resulting dark mixture was diluted with diethyl ether, and stirred at room temperature for 10 minutes. The mixture was filtered through a short silica gel column. The filtrate was concentrated in vacuo to give 4-benzyloxy-6-fluoro-3-methyl-naphthalene-2-carbaldehyde (165 mg, 93%) as a white solid, which was used in the next step without further purification. 1H NMR (400 MHz, CDCl3) δ ppm 10.31 (s, 1H), 8.16 (s, 1H), 8.00 (dd, J=8.84, 5.56 Hz, 1H), 7.73 (dd, J=10.48, 2.40 Hz, 1H), 7.55 (d, J=6.82 Hz, 2H), 7.39-7.49 (m, 2H), 7.32 (td, J=8.65, 2.65 Hz, 1H), 4.99 (s, 2H), 2.75 (s, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642629B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-cf2c744260664e2b98f4d6338dcc58f4 |
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| 출처 메모 | uspto-grants-2014_02 |
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