Ethanol → 1H-Indene-1,3(2H)-dione, 2-(3-methoxyphenyl)-

HRID 274213

反応式

HRID 274213 の反応式
[Na].O1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[CH2:4][C:3]1=[O:11].CO[C:14]1[CH:15]=[C:16]([CH:19]=[CH:20][CH:21]=1)[CH:17]=[O:18].O.[CH2:23]([OH:25])C>C(O)(=O)C>[CH3:23][O:25][C:9]1[CH:10]=[C:5]([CH:4]2[C:3](=[O:11])[C:19]3[C:16](=[CH:15][CH:14]=[CH:21][CH:20]=3)[C:17]2=[O:18])[CH:6]=[CH:7][CH:8]=1

参加物

7

反応物 5

HCID 702EthanolHCID 962WaterHCID 115693-MethoxybenzaldehydeHCID 683822(3H)-BenzofuranoneHCID 5360545Sodium

生成物 1

HCID 28178101H-Indene-1,3(2H)-dione, 2-(3-methoxyphenyl)-

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
20 °C

実験手順

Sodium (18.9 parts) was dissolved in absolute ethanol (380 parts) with stirring and was cooled to 20° C. and benzofuranone (100 parts) and 3-methoxybenzaldehyde were added. The reaction mixture was stirred under reflu for 15 minutes and cooled to 20° C. over 1 hour. The reaction mixture was poured into water (900 parts) and the ethanol was removed by evaporation under reduced pressure. Hydrochloric acid was added to the solution until acid and the aqueous phase was decanted to leave a red gum. The gum was dissolved in hot acetic acid (300 parts) and the solution was cooled to 20° C. and a solid was precipitated. The solid was isolated by filtration, washed with ethanol (74 OP) and dried to give 2-(3-methoxyphenyl)-1,3-indandione (55.8 parts) m.pt. 142°-144° C.

後処理

  1. stirringThe reaction mixture was stirred under reflu for 15 minutes
  2. temperaturecooled to 20° C. over 1 hour
  3. customthe ethanol was removed by evaporation under reduced pressure
  4. additionHydrochloric acid was added to the solution until acid
  5. customthe aqueous phase was decanted
  6. customto leave a red gum
  7. temperaturethe solution was cooled to 20° C.
  8. customa solid was precipitated
  9. customThe solid was isolated by filtration
  10. washwashed with ethanol (74 OP)
  11. customdried

出典と根拠

ORDレコード
ord-0f752959c2ce469186e19c06d23a269b
出典データセット
uspto-grants-1995_02
特許番号
US05389597

関連ノート

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