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2-(2,3-Dimethoxyphenyl)-4,4-dimethyl-4,5-dihydrooxazole → HCID 10243704、化合物

HRID 1250086
ノート
印刷プレビュー

反応式

HRID 1250086 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 111282672-(2,3-Dimethoxyphenyl)-4,4-dimethyl-4,5-dihydrooxazoleHCID 178418918HCID 178418918、化合物

生成物 1

HCID 10243704HCID 10243704、化合物収率 95.4%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-0cef4f51848a418d98be06d115324207
出典データセット
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06335459B1

反応ノート

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