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Acetone → 2-Methyl-4-methoxy-5-nitrophenyl mesylate

HRID 2050749
ノート
印刷プレビュー

反応式

HRID 2050749 の反応式
[CH3:1]C(C)=O.[S:5]([O:9][C:10]1[CH:15]=[C:14]([N+:16]([O-:18])=[O:17])[C:13]([OH:19])=[CH:12][C:11]=1[CH3:20])(=[O:8])(=[O:7])[CH3:6].C(=O)([O-])[O-].[Na+].[Na+].S(OC)(OC)(=O)=O>O>[S:5]([O:9][C:10]1[CH:15]=[C:14]([N+:16]([O-:18])=[O:17])[C:13]([O:19][CH3:1])=[CH:12][C:11]=1[CH3:20])(=[O:7])(=[O:8])[CH3:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 180AcetoneHCID 6497Dimethyl SulfateHCID 10340Sodium CarbonateHCID 198211444-Hydroxy-2-methyl-5-nitrophenyl methanesulfonate

生成物 1

HCID 198211562-Methyl-4-methoxy-5-nitrophenyl mesylate収率 77%

試薬・触媒・溶媒 1

HCID 962Water
溶媒

実験手順

To 200 ml of acetone, were added 19.1 g (77.3 mmol) of 2-methyl-4-hydroxy-5-nitrophenyl mesylate, 31.2 g of sodium carbonate and 19.2 g of dimethyl sulfate. The obtained mixture was heated under reflux for 3 hours. The reaction mixture was cooled and 700 ml of water was poured thereto. Then the mixture was extracted with 700 ml of chloroform, and the extract was washed with water and dried over anhydrous Glauber's salt. After distilling off the solvent under reduced pressure, the residue was recrystallized from a solvent mixture (hexane/acetone (2:1, by volume)) to thereby give 15.4 g (59.1 mmol) of 2-methyl-4-methoxy-5-nitrophenyl mesylate. The yield was 77%.

後処理

  1. temperatureThe obtained mixture was heated
  2. temperatureunder reflux for 3 hours
  3. temperatureThe reaction mixture was cooled
  4. extractionThen the mixture was extracted with 700 ml of chloroform
  5. washthe extract was washed with water
  6. dry with materialdried over anhydrous Glauber's salt
  7. distillationAfter distilling off the solvent under reduced pressure
  8. customthe residue was recrystallized from a solvent mixture (hexane/acetone (2:1, by volume))

出典と根拠

ORDレコード
ord-8fc84b271adc411a82d4a5cbbaca7941
出典データセット
uspto-grants-1991_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05015260

反応ノート

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