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Tetrahydrofuran → HCID 13620271, compound

HRID 1426497
Notes
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Reaction equation

HRID 1426497 reaction equation
[CH3:1][C:2](=[O:7])[CH2:3][C:4](=O)[CH3:5].COC(OC)[N:11]([CH3:13])C.O1CCCC1.Cl.Cl.[CH2:23]([NH:30]N)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>O.C(OCC)(=O)C>[CH2:23]([N:30]1[C:4]([CH3:5])=[C:3]([C:2](=[O:7])[CH3:1])[CH:13]=[N:11]1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 8028TetrahydrofuranHCID 31261AcetylacetoneHCID 78373Dimethylformamide dimethyl acetalHCID 146540Benzylhydrazine dihydrochloride

Product 1

HCID 13620271HCID 13620271, compoundYield 63.2%

Reagents, catalysts & solvents 2

HCID 962
Water
Solvent
HCID 8857Ethyl AcetateSolvent

Conditions

Temperature
80 °C

Procedure

A mixture of pentane-2,4-dione (10.01 g) and 1,1-dimethoxy-N,N-dimethylmethanamine (12.51 g) was stirred at 80° C. for 1 hr. Tetrahydrofuran (20 mL) was added to the reaction mixture, benzylhydrazine dihydrochloride (21.46 g) was added by small portions under ice-cooling, and the mixture was stirred at 60° C. for 30 min. The reaction mixture was allowed to cool to room temperature, ethyl acetate (100 mL) and water (100 mL) were added, and the separated aqueous layer was extracted with ethyl acetate (50 mL×2). The combined organic layers were washed with brine (20 mL) and dried over anhydrous magnesium sulfate. Insoluble material was removed by filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title to compound (13.53 g) as a colorless oil.

Workup

  1. additionwas added by small portions under ice-
  2. temperaturecooling
  3. stirringthe mixture was stirred at 60° C. for 30 min
  4. temperatureto cool to room temperature
  5. extractionthe separated aqueous layer was extracted with ethyl acetate (50 mL×2)
  6. washThe combined organic layers were washed with brine (20 mL)
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customInsoluble material was removed by filtration
  9. concentrationthe filtrate was concentrated under reduced pressure
  10. customthe residue was purified by silica gel column chromatography (ethyl acetate/hexane)

Sources & evidence

ORD record
ord-08fd69171e894c6db65a2ef9a7a3b267
Source dataset
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08933069B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes