Methanol → HCID 20312409, compound

HRID 1731039Notes

Reaction equation

HRID 1731039 reaction equation
C([O:5][C:6](=[O:24])[CH:7]([C:16]1[CH:21]=[CH:20][C:19]([OH:22])=[CH:18][C:17]=1[OH:23])[NH:8][C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])CCC.CO.C(=O)(O)[O-].[Na+]>O>[C:12]([O:11][C:9]([NH:8][CH:7]([C:16]1[CH:21]=[CH:20][C:19]([OH:22])=[CH:18][C:17]=1[OH:23])[C:6]([OH:24])=[O:5])=[O:10])([CH3:15])([CH3:13])[CH3:14]

Participants

5

Reactant 3

HCID 887MethanolHCID 516892Sodium BicarbonateHCID 20312442HCID 20312442, compound2×

Product 1

HCID 20312409HCID 20312409, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

To a boiling solution of 23 g. (0.067 mol.) of N-t-butoxycarbonyl-2-(2,4-dihydroxyphenyl)glycine n-butyl ester in 300 ml. of methanol was slowly added a solution of 23 g. of sodium bicarbonate in 300 ml. of water. During addition, the reaction mixture was kept under a nitrogen atmosphere and the methanol was allowed to distill from the mixture. When all the methanol had been distilled the mixture was cooled, adjusted to pH 7.0 with phosphoric acid and extracted with ethyl acetate. The aqueous phase was acidified to pH 4.0 and again extracted with ethyl acetate. The extract was dried (Na2SO4) and concentrated in vacuo to give the title compound.

Workup

  1. additionDuring addition
  2. distillationto distill from the mixture
  3. distillationWhen all the methanol had been distilled the mixture
  4. temperaturewas cooled
  5. extractionextracted with ethyl acetate
  6. extractionagain extracted with ethyl acetate
  7. dry with materialThe extract was dried (Na2SO4)
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-dde1c897e61d435ba548bec4be6a5163
Source dataset
uspto-grants-1976_11
Patent number
US03994954

Reaction notes

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