Methyl iodide → Methyl 9-methylxanthene-9-carboxylate

HRID 750549

反応式

HRID 750549 の反応式
[CH:1]1[C:14]2[CH:13]([C:15]([O:17][CH3:18])=[O:16])[C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[O:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[CH3:19]I>O1CCCC1.O>[CH3:19][C:13]1([C:15]([O:17][CH3:18])=[O:16])[C:14]2[CH:1]=[CH:2][CH:3]=[CH:4][C:5]=2[O:6][C:7]2[C:12]1=[CH:11][CH:10]=[CH:9][CH:8]=2

参加物

5

反応物 2

HCID 6328Methyl iodideHCID 699662methyl 9H-xanthene-9-carboxylate

生成物 1

HCID 12068831Methyl 9-methylxanthene-9-carboxylate

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒2 回

実験手順

9.61 g (0.04 mol) of methyl 9-xanthenecarboxylate (obtainable according to step 1.1.a) are dissolved in 150 mL of tetrahydrofuran, combined with a solution of 5.0 g (0.042 mol) potassium lert-butoxide in THF, and stirred for 10 minutes. 5 mL (0.08 mol) of methyl iodide are then added dropwise with gentle cooling; after all has been added, the mixture is stirred for 1 hour at ambient temperature. The reaction mixture is diluted with water to a total volume of 800 mL, extracted with diethyl ether, and the organic phase is extracted with saturated, aqueous Na2CO3 solution, washed with water, dried over magnesium sulfate, and the solvent is distilled off. The product is purified by recrystallization from methanol. Yield: 6.05 g of white crystals (70% of theoretical yield); melting point: 91° C.-92° C.

後処理

  1. additionafter all has been added
  2. stirringthe mixture is stirred for 1 hour at ambient temperature
  3. extractionextracted with diethyl ether
  4. extractionthe organic phase is extracted with saturated, aqueous Na2CO3 solution
  5. washwashed with water
  6. dry with materialdried over magnesium sulfate
  7. distillationthe solvent is distilled off
  8. customThe product is purified by recrystallization from methanol

出典と根拠

ORDレコード
ord-94e14b9758644a0fb58f5a01aa7563d7
出典データセット
uspto-grants-2008_07
特許番号
US07405224B2

関連ノート

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