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2-(2,3-Dimethoxyphenyl)-4,4-dimethyl-4,5-dihydrooxazole → HCID 10243704, 화합물

HRID 1250086
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HRID 1250086 반응식
[CH:1]([Mg]Cl)([CH3:3])[CH3:2].CO[C:8]1[C:13]([O:14][CH3:15])=[CH:12][CH:11]=[CH:10][C:9]=1[C:16]1[O:17][CH2:18][C:19]([CH3:22])([CH3:21])[N:20]=1>O1CCCC1>[CH:1]([C:8]1[C:13]([O:14][CH3:15])=[CH:12][CH:11]=[CH:10][C:9]=1[C:16]1[O:17][CH2:18][C:19]([CH3:21])([CH3:22])[N:20]=1)([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 111282672-(2,3-Dimethoxyphenyl)-4,4-dimethyl-4,5-dihydrooxazoleHCID 178418918HCID 178418918, 화합물

생성물 1

HCID 10243704HCID 10243704, 화합물수율 95.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Isopropylmagnesium chloride (2.0M in diethyl ether) (18.75 ml, 37.5 mmol) was added dropwise to a solution of 2-(2,3-dimethoxyphenyl)-4,4-dimethyl-4,5-dihydrooxazole (7.06 g, 30.0 mmol) in freshly distilled tetrahydrofuran at room temperature. The mixture was stirred overnight, quenched with water, and diluted with diethyl ether. The layers were separated, and the aqueous layer was washed twice with diethyl ether. The combined organic extracts were dried over anhydrous sodium sulfate, and concentrated in vacuo. Purification by silica gel flash chromatography, eluting with hexane/ethyl acetate, gave 2-(2-isopropyl-3-methoxyphenyl)-4,4-dimethyl-4,5-dihydrooxazole as a clear oil (7.08 g, 95.4%).

후처리

  1. customquenched with water
  2. additiondiluted with diethyl ether
  3. customThe layers were separated
  4. washthe aqueous layer was washed twice with diethyl ether
  5. dry with materialThe combined organic extracts were dried over anhydrous sodium sulfate
  6. concentrationconcentrated in vacuo
  7. customPurification by silica gel flash chromatography
  8. washeluting with hexane/ethyl acetate

출처 및 근거

ORD 기록
ord-0cef4f51848a418d98be06d115324207
출처 데이터셋
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06335459B1

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