참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydroxylamine HCl | HCID 21645 | — |
| 반응물 | (1-methyl-1H-tetrazol-5-yl)(phenyl)methanone | HCID 12331986 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | N-hydroxy-1-(1-methyl-1H-tetrazol-5-yl)-1-phenylmethanimine | HCID 135990939 | 100% |
반응 단계
(1-methyltetrazol-5-yl)phenylmethanone (11.1 g, 59.1 mmol) and hydroxylammonium chloride (10.3 g, 148 mmol) were added to 100 ml of pyridine, followed by stirring at 45° C. for 24 hours. After the completion of the reaction, the reaction solution was concentrated under reduced pressure and water and ethyl acetate were added to the resulting residue, and then the reaction product was extracted. The organic layer was washed in turn with dilute hydrochloric acid, water and an aqueous sodium hydrogencarbonate, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off from the organic layer to obtain (1-methyltetrazol-5-yl)phenylmethanoneoxime (12.0 g, yield: 100%) represented by the formua:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07183299B2 |
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| 출처 데이터셋 | uspto-grants-2007_02 |
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| ORD ID | ord-ed8ca4e8b684411eb7408c665a9f1654 |
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| 출처 메모 | uspto-grants-2007_02 |
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