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Hydrochloric Acid → 5-Benzyl-2-hydroxy-benzaldehyde

HRID 2057955
ノート
印刷プレビュー

反応式

HRID 2057955 の反応式
[OH-:1].[Na+].[CH2:3]([C:10]1[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH:17](Cl)(Cl)Cl.Cl>C(O)C.O>[CH2:3]([C:10]1[CH:11]=[C:12]([CH:17]=[O:1])[C:13]([OH:16])=[CH:14][CH:15]=1)[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 6212Chloroform2 回HCID 75634-BenzylphenolHCID 14798Sodium Hydroxide

生成物 1

HCID 45126705-Benzyl-2-hydroxy-benzaldehyde

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962
Water
溶媒

反応条件

温度
75 °C

実験手順

157 g of sodium hydroxide (50% in water) was added all at once to a stirred mixture of 100 g of p-benzylphenol in 165 ml of ethanol. The mixture was heated to 75°-80° C., and 161.5 g of chloroform was added drop-by-drop to the stirred mixture over a 5-hour period, at 75°-80° C., then was stirred for 2 hours at 75° C. Then 80.8 g of chloroform was added drop-by-drop, at 75°-80° C., and the mixture was stirred for 1 hour at 75° C. This procedure was repeated. The mixture was concentrated under reduced pressure to give a solid residue. The residue was poured into water, and the stirred mixture was acidified with concentrated hydrochloric acid. The aqueous phase was separated, extracted with ether and the extract was concentrated under reduced pressure to give an oil. The oil was extracted with petroleum ether. The extract was concentrated under reduced pressure. The residue was suspended in 150 ml of a saturated solution of sodium bisulfite and the mixture was stirred for 1 hour at room temperature. The liquid was decanted, and the solid was washed with water, stirred with ethanol and the mixture was filtered. The solid was washed with ether, then suspended in 10% sulfuric acid solution. The resulting mixture was stirred for 11/2 hours, then extracted with ether. The extract was dried (MgSO4) and concentrated under reduced pressure to give 5-benzylsalicylaldehyde (1A).

後処理

  1. temperatureThe mixture was heated to 75°-80° C.
  2. stirringthe mixture was stirred for 1 hour at 75° C
  3. concentrationThe mixture was concentrated under reduced pressure
  4. customto give a solid residue
  5. customThe aqueous phase was separated
  6. extractionextracted with ether
  7. concentrationthe extract was concentrated under reduced pressure
  8. customto give an oil
  9. extractionThe oil was extracted with petroleum ether
  10. concentrationThe extract was concentrated under reduced pressure
  11. stirringthe mixture was stirred for 1 hour at room temperature
  12. customThe liquid was decanted
  13. washthe solid was washed with water
  14. stirringstirred with ethanol
  15. filtrationthe mixture was filtered
  16. washThe solid was washed with ether
  17. stirringThe resulting mixture was stirred for 11/2 hours
  18. extractionextracted with ether
  19. dry with materialThe extract was dried (MgSO4)
  20. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-2b500a1084364936b6316fdaa053a0b8
出典データセット
uspto-grants-1980_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04213999

反応ノート

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