Ethanol → Ethyl 3-(1-naphthyl)propanoate

HRID 1779390ノート

反応式

HRID 1779390 の反応式
[C:1]1([CH2:11][CH2:12][C:13]([OH:15])=[O:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[CH2:16](O)[CH3:17]>S(=O)(=O)(O)O>[C:1]1([CH2:11][CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1

参加物

4

反応物 2

HCID 702EthanolHCID 952541-Naphthalenepropionic acid

生成物 1

HCID 10966256Ethyl 3-(1-naphthyl)propanoate

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid触媒

実験手順

A stirred solution of 50 grams (0.25 mole) of 3-(naphth-1-yl) propanoic acid and 20 drops (catalyst) of concentrated sulfuric acid in 250 mL of ethanol was heated at reflux for about 24 hours. After this time the reaction mixture was concentrated under reduced pressure to a residue. The residue was dissolved in diethyl ether, and the solution was washed with two 150 mL portions of an aqueous solution saturated with sodium bicarbonate and then with 150 mL of an aqueous solution saturated with sodium chloride. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 56.0 grams of ethyl 3-(naphth-1-yl)propanoate. The NMR spectrum was consistent with the proposed structure.

後処理

  1. temperatureat reflux for about 24 hours
  2. concentrationAfter this time the reaction mixture was concentrated under reduced pressure to a residue
  3. dissolutionThe residue was dissolved in diethyl ether
  4. washthe solution was washed with two 150 mL portions of an aqueous solution saturated with sodium bicarbonate
  5. dry with materialThe organic layer was dried with magnesium sulfate
  6. filtrationfiltered
  7. concentrationThe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-c767b76b59c2438e96aa9b5b60875fad
出典データセット
uspto-grants-1997_05
特許番号
US05627189

反応ノート

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