Hydrochloric Acid → 2',4'-dihydroxy-3'-prenylacetophenone

HRID 2254200ノート

反応式

HRID 2254200 の反応式
[OH:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:11])[CH3:10].C(=O)([O-])[O-].[K+].[K+].Cl[CH2:19][CH:20]=[C:21]([CH3:23])[CH3:22].Cl>O1CCCC1>[OH:1][C:2]1[C:7]([CH2:19][CH:20]=[C:21]([CH3:23])[CH3:22])=[C:6]([OH:8])[CH:5]=[CH:4][C:3]=1[C:9](=[O:11])[CH3:10]

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 69902',4'-DihydroxyacetophenoneHCID 104291-Chloro-3-methyl-2-buteneHCID 11430Potassium Carbonate

生成物 1

HCID 109329712',4'-dihydroxy-3'-prenylacetophenone収率 45.4%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

In 750 ml of tetrahydrofuran was dissolved 149.95 g of 2',4'-dihydroxyacetophenone, and 409.26 g of anhydrous potassium carbonate and 150 ml of 1-chloro-3-methyl-2-butene were added to the solution and the mixture was stirred at room temperature in a nitrogen current for 5 days. After the reaction, 3 N hydrochloric acid was added to the reaction liquid under cooling to make the aqueous layer acidic, and the aqueous layer was extracted with ether. The ether extract was washed with water and dried with anhydrous sodium sulfate and the solvent was removed by distillation. Then, 800 ml of hexane was added to the obtained residue and the hexane-soluble substances were removed by decantation to obtain 98.55 g (yield=45.4%) of 2',4'-dihydroxy-3'-(3-methyl-2-butenyl)acetophenone in the form of a colorless solid.

後処理

  1. additionwere added to the solution
  2. additionwas added to the reaction liquid
  3. temperatureunder cooling
  4. extractionthe aqueous layer was extracted with ether
  5. extractionThe ether extract
  6. washwas washed with water
  7. dry with materialdried with anhydrous sodium sulfate
  8. customthe solvent was removed by distillation
  9. additionThen, 800 ml of hexane was added to the obtained residue
  10. customthe hexane-soluble substances were removed by decantation

出典と根拠

ORDレコード
ord-46c4b2d03b6c47eea626bd75ff00d8cc
出典データセット
uspto-grants-1993_08
特許番号
US05234951

反応ノート

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