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Triacetoxyperiodinane → 1-(6-Methoxy-2-methylpyridin-3-yl)propan-1-one

HRID 1671324
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HRID 1671324 반응식
[CH3:1][O:2][C:3]1[N:8]=[C:7]([CH3:9])[C:6]([CH:10]([OH:13])[CH2:11][CH3:12])=[CH:5][CH:4]=1.CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.C([O-])(O)=O.[Na+]>C(Cl)Cl>[CH3:1][O:2][C:3]1[N:8]=[C:7]([CH3:9])[C:6]([C:10](=[O:13])[CH2:11][CH3:12])=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 159087TriacetoxyperiodinaneHCID 516892Sodium BicarbonateHCID 67336369HCID 67336369, 화합물

생성물 1

HCID 673358811-(6-Methoxy-2-methylpyridin-3-yl)propan-1-one

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of 1-(6-methoxy-2-methyl-pyridin-3-yl)-propan-1-ol (1.15 g, 6.35 mmol) in DCM (20 ml) is treated with Dess-Martin periodinane (2.96 g, 6.98 mmol) and the resulting suspension stirred at RT overnight. The reaction mixture is diluted with DCM (80 ml) and sat NaHCO3 (50 ml) added. The organic layer is separated and washed with H2O (20 ml), brine (20 ml), dried (MgSO4) and concentrated in vacuo. The resulting residue is purified by chromatography on silica gel (2×70 ml) using 50% EtOAc/iso-hexane to give 1-(6-methoxy-2-methyl-pyridin-3-yl)-propan-1-one as a white solid. MS: m/z 180.2 [M+H]+.

후처리

  1. additionadded
  2. customThe organic layer is separated
  3. washwashed with H2O (20 ml), brine (20 ml)
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customThe resulting residue is purified by chromatography on silica gel (2×70 ml)

출처 및 근거

ORD 기록
ord-e977fea0ae304aa68bbb129b9bab52c0
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07994203B2

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