Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63075생성일: 2026년 10월 25일
6-Methoxy-alpha-tetralone → 1-(Aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol
https://huagongshe.com/reaction/63075
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 6-Methoxy-alpha-tetralone | HCID 14112 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Trimethylsilyl cyanide | HCID 82115 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 촉매 | zinc(II)iodide | HCID 9883512 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 1-(Aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol | HCID 13197589 | 68.4% |
반응 단계
TMS-cyanide (8.52 mL, 68.1 mmol) was added to a solution of 6-methoxy-1-tetralone (6.0 g, 34 mmol) in toluene (50 mL). A trace amount (˜20 mg) of zinc iodide was added, and the reaction was stirred at 60° C. for 16 hours. The solution was cooled to rt and diluted with THF (30 mL). This was added to a mixture of lithium aluminum hydride (2.58 g) in THF (50 mL), and the reaction mixture was heated at 42° C. for 2 h. The reaction was cooled to rt. EtOAc (10 mL) was slowly added, and the reaction stirred 30 min. Water (2 mL) and then 5N NaOH (1 mL) were slowly added, and the reaction stirred 1 h. The reaction mixture was diluted with EtOAc (100 mL), dried (MgSO4), and filtered through Celite. Purification by silica gel chromatography (10-20% MeOH/DCM) gave 4.82 g of 1-(aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-ol as a clear oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09447045B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-060b901605a7488ead9bd01c7620fa71 |
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| 출처 메모 | uspto-grants-2016_09 |
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