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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

반응식

참여 물질

역할이름HCID투입량
반응물6-Methoxy-alpha-tetraloneHCID 14112—
반응물Sodium HydroxideHCID 14798—
반응물Trimethylsilyl cyanideHCID 82115—
반응물Aluminium lithium hydrideHCID 21226445—
촉매zinc(II)iodideHCID 9883512—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-(Aminomethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-1-olHCID 1319758968.4%

반응 조건

온도60 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447045B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-060b901605a7488ead9bd01c7620fa71
출처 메모uspto-grants-2016_09