참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 2,4,6-Trimethoxybenzaldehyde | HCID 70019 | — |
| 반응물 | O-Benzylhydroxylamine | HCID 102313 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | O-benzyl-N-(2,4,6-trimethoxy-benzyl)hydroxylamine | HCID 22494979 | 83% |
반응 단계
2,4,6-Trimethoxybenzaldehyde (12.42 g, 63.3 mmol) and O-benzylhydroxylamine (7.80 g, 63.3 mmol) were stirred in dichloromethane (65 mL) at rt overnight. The solvent was removed under reduced pressure. The crude residue was dissolved in ethanol (550 mL) and sodium cyanoborohydride (12.0 g, 189.9 mmol) was added dropwise. The mixture was stirred for 5-10 min, then 12 N HCl was added dropwise until pH became below 3. The reaction mixture was stirred for additional 3 h and 1 N NaOH was added until pH>8. The product was extracted with dichloromethane. The organic phase was dried over Na2SO4 and concentrated under vacuo. The residue was purified by flash chromatography (5% ether in dichloromethane) to give 15.9 g of O-benzyl-N-(2,4,6-trimethoxy-benzyl)hydroxylamine as an oil (83% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06884907B2 |
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| 출처 데이터셋 | uspto-grants-2005_04 |
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| ORD ID | ord-c82029e8226e4b60aef08c7dc6342d43 |
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| 출처 메모 | uspto-grants-2005_04 |
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