Réaction #550890
ord-35d47ebdff3e4476a21a56f8a62db778
Équation de réaction
Réactifs
Réactifs
Conditions de réaction
Traitement
- 1Températurewas cooled to 0°
- 2Autreevaporation to dryness]
- 3workup.ADDITIONwas added concurrently with 4N sodium hydroxide maintaining a pH of 7.0-8.0
- 4workup.ADDITIONUpon completion of the acid chloride addition
- 5Températurethe pH was maintained at 9.0 for 1 hour
- 6AutreThe layers were separated
- 7Extractionthe aqueous layer extracted once with methylene chloride
- 8LavageThe combined organic layers were washed once with excess saturated sodium bicarbonate solution
- 9Séchagedried over sodium sulfate
- 10Autreevaporated in vacuo
Mode opératoire
A mixture of 289 g of alpha-(aminomethyl)-3,4-dimethoxybenzeneacetic acid ethyl ester hydrochloride, 1000 ml of methylene chloride and 1000 ml of water was cooled to 0° and adjusted to pH 9.0 with 4N sodium hydroxide. A solution of 1000 ml of methylene chloride and 3,4-dimethoxyphenyl acetic acid chloride [previously prepared by the action of 400 ml of thionyl chloride on 215 g of 3,4-dimethoxyphenyl acetic acid in 500 ml of toluene at 50° for 1 hour and evaporation to dryness] was added concurrently with 4N sodium hydroxide maintaining a pH of 7.0-8.0. Upon completion of the acid chloride addition, the pH was maintained at 9.0 for 1 hour followed by acidification to pH 1.0 with 6N hydrochloric acid. The layers were separated and the aqueous layer extracted once with methylene chloride. The combined organic layers were washed once with excess saturated sodium bicarbonate solution, dried over sodium sulfate and evaporated in vacuo to give 430 g of 2-(3,4-dimethoxyphenyl)-3-{{[(3,4-dimethoxyphenyl)methyl]carbonyl}amino}propanoic acid ethyl ester as an oil.