Hydrochloric Acid → HCID 22239057, compound

HRID 1743344

Reaction equation

HRID 1743344 reaction equation
[OH-:1].[Li+].[CH3:3][C:4]([C:6]1[CH:7]=[CH:8][C:9](O)=[CH:10][C:11]=1[OH:12])=[O:5].[CH:14]1[C:26]2[C:25](=[O:27])[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[C:18]=2[C:17]([C:28](Cl)=O)=[CH:16][CH:15]=1.Cl>C1COCC1>[CH:14]1[C:26]2[C:25](=[O:27])[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[C:18]=2[C:17]([C:28]2[O:12][C:11]3[C:6]([C:4](=[O:5])[C:3]=2[OH:1])=[CH:7][CH:8]=[CH:9][CH:10]=3)=[CH:16][CH:15]=1

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 69902',4'-DihydroxyacetophenoneHCID 6101429-Fluorenone-4-carbonyl chloride

Product 1

HCID 22239057HCID 22239057, compound

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
-10 °C

Procedure

Dry, pulverulent lithium hydroxide (11.55 mmol, 3.3 equivalents) is added in one portion to a well-stirred solution of 2,4-dihydroxyacetophenone (3.22 mmol) in dry THF (5 ml) under an argon atmosphere at −78° C. The reaction mixture is stirred at −78° C. for one hour and subsequently at −10° C. for two hours. After the mixture has been re-cooled to −78° C., a solution of 9-fluorenone-4-carbonyl chloride (3.3 mmol) in THF (10 ml) is added in one portion. The mixture is stirred at −78° C. for one hour and at room temperature for 4 hours until the starting material has disappeared. The reaction mixture is emptied into a mixture of ice (150 g) and concentrated HCl (5 ml) and extracted with chloroform (3×50 ml). The solvents are removed from the dried extracts, and the residue is dried under reduced pressure for 24 hours. Glacial acetic acid (30 ml) and sulfuric acid (0.2 ml) are added to the residue, and the mixture is heated at 95–100° C. for from 30 minutes to one hour under an argon atmosphere. Approximately one third of the acetic acid is stripped off, and the residue is emptied into water. The precipitated product is filtered, washed and dried and recrystallised in methanol, giving 2-(9-fluorenon-4-yl)hydroxychromone. EI-MS (70 eV) m/e (rel. abund.)=340.

Workup

  1. customDry
  2. temperatureAfter the mixture has been re-cooled to −78° C.
  3. stirringThe mixture is stirred at −78° C. for one hour and at room temperature for 4 hours until the starting material
  4. extractionextracted with chloroform (3×50 ml)
  5. customThe solvents are removed from the dried extracts
  6. customthe residue is dried under reduced pressure for 24 hours
  7. additionGlacial acetic acid (30 ml) and sulfuric acid (0.2 ml) are added to the residue
  8. temperaturethe mixture is heated at 95–100° C. for from 30 minutes to one hour under an argon atmosphere
  9. filtrationThe precipitated product is filtered
  10. washwashed
  11. customdried
  12. customrecrystallised in methanol

Sources & evidence

ORD record
ord-b9219aab03b241509d7cd8cb7a69d0ef
Source dataset
uspto-grants-2006_03
Patent number
US07009062B2

Linked notes

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