참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | 4-(4-(Trifluoromethyl)benzyloxy)pyridine 1-oxide | HCID 68657649 | — |
| 생성물 | 4-(4-(trifluoromethyl)benzyloxy)pyridin-2(1H)-one | HCID 57950480 | 91% |
반응 단계
4-(4-(Trifluoromethyl)benzyloxy)pyridine 1-oxide (600 mg, 2.22 mmol) was heated to 140° C. in acetic anhydride (20 mL) for 2 h. The mixture was concentrated and then heated at 80° C. for 1 h in a mixture of MeOH (10 mL) and aqueous 1 N NaOH (10 mL). The resultant black solution was concentrated to a volume of 10 mL and extracted with CHCl3/EtOH (3:1). The organic layer was removed and concentrated to provide the title compound (550 mg, 91%) as a tan solid: 1H NMR (300 MHz, CD3OD) δ 7.70-7.60 (m, 4H), 7.41 (d, J=7.0 Hz, 1H), 6.17 (dd, J=7.0, 2.5 Hz, 1H), 5.96 (d, J=2.4 Hz, 1H), 5.18 (s, 2H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09296743B2 |
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| 출처 데이터셋 | uspto-grants-2016_03 |
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| ORD ID | ord-0c740a6f9da54177bb895d4fbbff3e89 |
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| 출처 메모 | uspto-grants-2016_03 |
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