[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:10]([C:12]([OH:14])=[O:13])[NH2:11])[CH:6]=[CH:7][C:8]=1[OH:9].Cl.[CH3:16]O>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:10]([C:12]([O:14][CH3:16])=[O:13])[NH2:11])[CH:6]=[CH:7][C:8]=1[OH:9]A cooled suspension of 94 g. (0.476 mole) of 2-(3'-methoxy-4'-hydroxyphenyl)glycine in 500 ml. of absolute methanol was gassed at a rapid rate with HCl for 20 minutes. At first a clear solution was obtained and then crystalline product separated in quantity. After 20 hours the methyl ester hydrochloride was filtered and washed sparingly with methanol; 99.6 g. after air drying. A cooled solution of the hydrochloride in 800 ml. of water was adjusted to pH 8 (NaOH) giving a crystalline precipitate of the ester free base; 81.3 g. The IR and NMR spectra were consistent.
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