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Methyl iodide → N-(Benzyloxy)methanamine--hydrogen chloride (1/1)

HRID 2180237
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HRID 2180237 반응식
[ClH:1].[CH2:2]([O:9][NH2:10])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:11](OC(OC(C)(C)C)=O)(OC(C)(C)C)=O.CN1CCOCC1.CI.[H-].[Na+]>ClCCl.CCOCC.C1COCC1>[ClH:1].[CH3:11][NH:10][O:9][CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 5

HCID 6328Methyl iodideHCID 79724-MethylmorpholineHCID 24758Sodium hydrideHCID 90495Di-tert-butyl dicarbonateHCID 102312Benzyloxyamine hydrochloride

생성물 1

HCID 13417388N-(Benzyloxy)methanamine--hydrogen chloride (1/1)

시약·촉매·용매 3

HCID 3283
Diethyl Ether
용매
HCID 6344Dichloromethane용매
HCID 8028Tetrahydrofuran용매

실험 절차

O-Benzylhydroxylamine hydrochloride (1.59 g, 0.01 mol), di-tert-butyl dicarbonate (2.18 g, 0.01 mol) and N-methyl morpholine (1.1 mL, 0.01 mol) in dichloromethane (40 mL) were stirred at room temperature for 16 hours. The reaction mixture was diluted with ether, washed with 10% NaHSO4, then brine, dried over (Na2SO4), and concentrated. The residue was treated with methyl iodide (1.6 mL, 0.025 mmol) in the presence of NaH (0.4 g, 0.01 mol) in THF at 0° C., then stirred at room temperature for 16 hours. The reaction was quenched with 1N HCl, diluted with ether, washed with brine, dried (Na2SO4), concentrated, purified by silica gel chromatography (20:80/ethyl acetate:hexanes) and treated with 4M HCl in dioxane to give the title compound.

후처리

  1. washwashed with 10% NaHSO4
  2. dry with materialbrine, dried over (Na2SO4)
  3. concentrationconcentrated
  4. customThe reaction was quenched with 1N HCl
  5. additiondiluted with ether
  6. washwashed with brine
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated
  9. custompurified by silica gel chromatography (20:80/ethyl acetate:hexanes)
  10. additiontreated with 4M HCl in dioxane

출처 및 근거

ORD 기록
ord-42e20d1918c64ee895595fe71d8bfe3a
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06887863B2

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