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1,4-Dioxane → 1-(Methoxymethyl)-3-oxocyclobutane-1-carbonitrile

HRID 1692921
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HRID 1692921 반응식
[O:1]1CCOCC1.[CH3:7][O:8][CH2:9][C:10]1([C:15]#[N:16])[CH2:13][C:12](=C)[CH2:11]1.I([O-])(=O)(=O)=O.[Na+]>O.[Os](=O)(=O)(=O)=O>[CH3:7][O:8][CH2:9][C:10]1([C:15]#[N:16])[CH2:13][C:12](=[O:1])[CH2:11]1
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참가 물질

6

반응물 3

HCID 312751,4-DioxaneHCID 23667635Sodium periodateHCID 668243071-(Methoxymethyl)-3-methylidenecyclobutane-1-carbonitrile

생성물 1

HCID 668243301-(Methoxymethyl)-3-oxocyclobutane-1-carbonitrile

시약·촉매·용매 2

HCID 30318Osmium Tetroxide촉매HCID 962Water용매
2회

실험 절차

A mixture of water (2 mL, 0.1 mol) and 1,4-dioxane (7 mL, 0.08 mol), 1-(methoxymethyl)-3-methylenecyclobutanecarbonitrile (0.294 g, 0.00214 mol), and 0.2 M of osmium tetraoxide in water (0.04 mL) was stirred for 5 min, during which time the mixture became brown. While the temperature was maintained at room temperature, sodium periodate (0.963 g, 0.00450 mol) was added in portions over a period of 30 min. The mixture was stirred overnight. The mixture was extracted with EtOAc and the combined organic layers were dried over MgSO4. After removal of the solvents, the crude product was used directly in next step (298 mg, 99.92%). 1H NMR (400 MHz, CDCl3): 3.70 (2H, s), 3.68 (3H, s), 3.58 (2H, m), 3.38 (2H, m) ppm.

후처리

  1. stirringThe mixture was stirred overnight
  2. extractionThe mixture was extracted with EtOAc
  3. dry with materialthe combined organic layers were dried over MgSO4
  4. customAfter removal of the solvents

출처 및 근거

ORD 기록
ord-8ea74a97d5ac4d97a808eaf3bc540c3b
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08158616B2

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