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Methanol → HCID 68502921, compound

HRID 1176317
Notes
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Reaction equation

HRID 1176317 reaction equation
[CH3:1][C:2]1[C:10]2[O:9][C:8]([C:11]([OH:13])=[O:12])=[CH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.[CH3:14]O>OS(O)(=O)=O>[CH3:1][C:2]1[C:10]2[O:9][C:8]([C:11]([O:13][CH3:14])=[O:12])=[CH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 887MethanolHCID 203039687-Methyl-1-benzofuran-2-carboxylic acid

Product 1

HCID 68502921HCID 68502921, compound

Reagents, catalysts & solvents 1

HCID 1118Sulfuric AcidSolvent

Procedure

A solution of 4.32 g of 7-methylbenzofuran-2-carboxylic acid in 150 ml of methanol and 1 ml of conc. H2SO4 is stirred at reflux over 9 hours. The reaction mixture is cooled and concentrated by evaporation. The residue is dissolved in diethyl ether and washed with water, saturated aqueous sodium hydrogencarbonate solution and brine, dried over sodium sulphate and concentrated by evaporation. The crude title compound is obtained as a red-brown oil from the residue. Rf=0.32 (1:6 EtOAc-heptane); Rt=4.51.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  1. temperatureat reflux over 9 hours
  2. temperatureThe reaction mixture is cooled
  3. concentrationconcentrated by evaporation
  4. dissolutionThe residue is dissolved in diethyl ether
  5. washwashed with water, saturated aqueous sodium hydrogencarbonate solution and brine
  6. dry with materialdried over sodium sulphate
  7. concentrationconcentrated by evaporation

Sources & evidence

ORD record
ord-1457b75f028c47ce852ebfebff9cae80
Source dataset
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07842688B2

Reaction notes

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