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Diethyl Ether → HCID 12641422、化合物

HRID 2239610
ノート
印刷プレビュー

反応式

HRID 2239610 の反応式
[C:1]1([CH3:12])[CH:6]=[C:5]([CH3:7])[CH:4]=[C:3]([CH3:8])[C:2]=1[CH2:9][CH:10]=[O:11].C[Mg+].[Br-].[CH3:16]COCC>C1COCC1>[C:3]1([CH3:8])[CH:4]=[C:5]([CH3:7])[CH:6]=[C:1]([CH3:12])[C:2]=1[CH2:9][CH:10]([OH:11])[CH3:16]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3283Diethyl EtherHCID 3003822-(2,4,6-Trimethylphenyl)acetaldehydeHCID 178418689HCID 178418689、化合物

生成物 1

HCID 12641422HCID 12641422、化合物収率 68.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Mesitylacetaldehyde (0.68 g, 4.19 mmol) was dissolved in THF (5.0 mL, dry) and MeMgBr in Et2O (3.0M, 0.75 g, 6.29 mmol)) was added slowly at 0° C. The cooling bath was removed and the reaction mixture was stirred at rt for 4.5 h. The mixture was cooled to 0° C. and excess Grignard reagent was hydrolyzed with HCl (1N). The mixture was diluted with water and extracted with Et2O. The organic layer was dried over Na2SO4, evaporated and the residue was purified by column chromatography on silica gel using MTBE, heptane and DCM as eluant giving the title compound (0.51 g, 61%). 1H NMR (CDCl3, 500 MHz) δ 6.88-6.85 (m, 2H), 4.08-3.99 (m, 1H), 2.87-2.72 (m, 2H), 2.32 (s, 6H), 2.26 (s, 3H), 1.29 (d, 3H).

後処理

  1. customThe cooling bath was removed
  2. temperatureThe mixture was cooled to 0° C.
  3. additionThe mixture was diluted with water
  4. extractionextracted with Et2O
  5. dry with materialThe organic layer was dried over Na2SO4
  6. customevaporated
  7. customthe residue was purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-3cfe10ff1c354cf49037b81be76757ea
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07723333B2

反応ノート

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