Methanol → Methyl Aminolevulinate Hydrochloride

HRID 2056647Notes

Reaction equation

HRID 2056647 reaction equation
[ClH:1].[NH2:2][CH2:3][C:4](=[O:10])[CH2:5][CH2:6][C:7]([OH:9])=[O:8].[CH3:11]O>>[ClH:1].[NH2:2][CH2:3][C:4](=[O:10])[CH2:5][CH2:6][C:7]([O:9][CH3:11])=[O:8]

Participants

3

Reactant 2

HCID 887MethanolHCID 123608Aminolevulinic Acid Hydrochloride

Product 1

HCID 157921Methyl Aminolevulinate Hydrochloride

Conditions

Temperature
60 °C

Procedure

To a 500 ml glass reactor containing 200 ml methanol, was added 1 g 5-amino-levulinic acid hydrochloride and 1 drop conc. HC 1. The reaction mixture was then stirred overnight at 60° C. The progress of the esterification was followed by 1H-NMR. Excess methanol was removed by distillation, and the product further dried under vacuum at 30-40° C., giving methyl 5-aminolevulinate hydrochloride. The structure was confirmed by 1H-NMR in DMSO-d6.

Workup

  1. customExcess methanol was removed by distillation
  2. customthe product further dried under vacuum at 30-40° C.

Sources & evidence

ORD record
ord-602352ec450d406a8b2ee039e1ae0b5e
Source dataset
uspto-grants-2008_02
Patent number
US07335684B2

Reaction notes

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