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Water → 4-Methoxy-3-isochromanone

HRID 428001
ノート
印刷プレビュー

反応式

HRID 428001 の反応式
C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1.[CH3:18][O:19][CH:20]([C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=1[CH2:32][O:33][CH:34]1CCCC[O:35]1)C(OCC)=O.O>CO>[CH3:18][O:19][CH:20]1[C:26]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[CH2:32][O:33][C:34]1=[O:35]
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 962WaterHCID 466102Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 18357803Ethyl alpha-methoxy-2-(tetrahydropyran-2-yloxymethyl)phenylacetate

生成物 1

HCID 155472854-Methoxy-3-isochromanone収率 74.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Pyridinium p-toluenesulfonate (0.30 g) was added to a solution of ethyl α-methoxy-2-(tetrahydropyran-2-yloxy-methyl)phenylacetate (14.00 g, 45.4 mmol) in methanol (50 ml), and the mixture was heated under reflux for 1 hour. The mixture was cooled to room temperature, and water (50 ml) was added. The mixture was extracted with methylene chloride and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by recrystallization from n-hexane/ethyl acetate (=1/1) to give the desired compound 4-methoxy-3-isochromanone (6.00 g, 74.2%) as white crystals.

後処理

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 1 hour
  3. extractionThe mixture was extracted with methylene chloride
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customThe solvent was evaporated
  6. customthe residue was purified by recrystallization from n-hexane/ethyl acetate (=1/1)

出典と根拠

ORDレコード
ord-c6be83fe0a194232a764a2067c2d6603
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06313150B1

反応ノート

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