Ethanol → 3-Methyl-6-(phenylthio)-phenylacetic acid

HRID 435609ノート

反応式

HRID 435609 の反応式
[CH3:1][C:2]1[CH:3]=[C:4](CC#N)[C:5]([S:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:6][CH:7]=1.[CH2:18]([OH:20])[CH3:19].[OH-:21].[K+]>O>[CH3:1][C:2]1[CH:3]=[C:4]([CH2:19][C:18]([OH:21])=[O:20])[C:5]([S:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:6][CH:7]=1

参加物

5

実験手順

500 g of 3-methyl-6-(phenylthio)-phenylacetonitrile, 1.2 litres of ethanol, 470 g of potassium hydroxide and 500 ml of water are heated for 12 hours under reflux. Then the ethanol is evaporated off under reduced pressure. The residue is treated with water until completely dissolved and the neutral constituents are extracted with benzene. The aqueous solution is filtered with the addition of some dicalite and active carbon, cooled and adjusted to pH 3 with concentrated hydrochloric acid. The mixture is then extracted three times with 1 litre of chloroform each time and the extracts are washed with water, dried over calcium chloride, filtered and concentrated under reduced pressure. The crude 3-methyl-6-(phenylthio)-phenylacetic acid obtained is recrystallised from benzene/hexane; melting point 132°-135° C.

後処理

  1. temperatureunder reflux
  2. customThen the ethanol is evaporated off under reduced pressure
  3. additionThe residue is treated with water
  4. dissolutionuntil completely dissolved
  5. extractionthe neutral constituents are extracted with benzene
  6. filtrationThe aqueous solution is filtered with the addition of some dicalite and active carbon
  7. temperaturecooled
  8. extractionThe mixture is then extracted three times with 1 litre of chloroform each time
  9. washthe extracts are washed with water
  10. dry with materialdried over calcium chloride
  11. filtrationfiltered
  12. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-c28e7ea782a94a0f97cb869f3c4acad3
出典データセット
uspto-grants-1977_02
特許番号
US04006145

反応ノート

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