참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2,3-Dimethoxybenzaldehyde | HCID 66581 | — |
| 반응물 | 2-Amino-1-(3,4-dimethoxyphenyl)ethan-1-ol hydrochloride | HCID 12888909 | — |
| 반응물 | HCID 178418435 | HCID 178418435 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | Veratryl alcohol | HCID 7118 | — |
반응 단계
1.0 g of α-(aminomethyl)-3,4-dimethoxybenzyl alcohol hydrochloride was suspended in 5 ml of methanol, and after adding thereto 0.85 g of 2,3-dimethoxybenzaldehyde, 0.63 ml of triethylamine was added dropwise to the mixture while stirring at room temperature. The mixture was heated under reflux for 30 minutes, and 0.24 g of sodium boron hydride was added slowly to the mixture while stirring under ice cooling. After the foaming stopped, the mixture was concentrated. The residue was subjected to a separating procedure with chloroform and water, the chloroform layer was collected, washed with water, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was recrystallized from ethyl acetate-n-hexane, giving 1.07 g of α-[[2,3-dimethoxybenzyl)amino]methyl]-3,4-dimethoxybenzyl alcohol, m.p. 96°-97° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05623074 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-3bcdb4656b234fc0b193760fcf8acf5b |
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| 출처 메모 | uspto-grants-1997_04 |
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