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Water → 1-Methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline

HRID 481781
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HRID 481781 반응식
[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([N+:12]([O-:14])=[O:13])[CH:10]=2)[CH2:5][CH2:4][N:3]=1.[BH4-].[Na+].O>CO>[CH3:1][CH:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([N+:12]([O-:14])=[O:13])[CH:10]=2)[CH2:5][CH2:4][NH:3]1
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참가 물질

5

반응물 3

HCID 962WaterHCID 4311764Sodium borohydrideHCID 109322281-Methyl-7-nitro-3,4-dihydroisoquinoline

생성물 1

HCID 215843111-Methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline수율 82.5%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

1.08 g of 1-methyl-7-nitro-3,4-dihydroisoquinoline was dissolved in 10 ml of methanol, and 0.43 g of sodium borohydride was added to the solution at 0° C. The solution was stirred overnight at room temperature, and water was added to the reaction mixture. The mixture was extracted with ethyl acetate, and after washing with saturated aqueous solution of sodium chloride, the solution was dried with anhydrous sodium sulfate. The desiccant was separated by filtration, and the filtrate was purified by silica gel column chromatography to obtain 0.90 g of 1-methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline, which was an oily product (yield: 82%).

후처리

  1. extractionThe mixture was extracted with ethyl acetate
  2. washafter washing with saturated aqueous solution of sodium chloride
  3. dry with materialthe solution was dried with anhydrous sodium sulfate
  4. customThe desiccant was separated by filtration
  5. customthe filtrate was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-a27e714908bf4ba4b1cf51f6fb4b7765
출처 데이터셋
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05789595

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