참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Iodine | HCID 807 | — |
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | 3-Phenylpropylformamide | HCID 12147094 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-Methyl-3-phenylpropan-1-amine | HCID 35417 | 53% |
반응 단계
N-(3-Phenylpropyl)formamide (5.70 g, 34.9 mmol) was dissolved in tetrahydrofuran (50 ml) and added dropwise to a suspension of sodium borohydride (1.58 g, 41.91 mmol) in tetrahydrofuran (100 ml), which was cooled to 7° C. A solution of iodine (4.42 g, 17.46 mmol) in tetrahydrofuran was added dropwise, while the temperature was kept at 7° C. After the addition was finished, the reaction mixture was warmed to reflux for 16 h. The reaction mixture was cooled to 7° C., and methanol (250 ml) was added dropwise. The solvent was removed in vacuo. The residue was dissolved in 20% aqueous sodium hydroxide solution (250 ml) and tert-butyl methyl ether (100 ml). The phases were separated. The aqueous phase was extracted with tert-butyl methyl ether (2×100 ml). The combined organic layers were dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (400 g), using dichicromethane/methanol/25% aqueous ammonia (100:10:1) as eluent to give 2.76 g of N-methyl-N-(3-phenylpropyl)amine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06274584B1 |
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| 출처 데이터셋 | uspto-grants-2001_08 |
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| ORD ID | ord-2b95b98d15cd46cfa6b107d261dde89f |
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| 출처 메모 | uspto-grants-2001_08 |
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