تفاعل #4515

ord-8f9ba23024a24c68b03865b18a945605

معادلة التفاعل

[OH-]
hydroxide
COC(=O)c1cc(N)cc(C(=O)OC)c1
dimethyl-5-amino-benzene-1,3-dicarboxylate
O=N[O-].[Na+]
sodium nitrite
O=C(O)Cc1ccccc1O
2-hydroxy-phenylacetic acid
COC(=O)c1cc(N=Nc2ccc(O)c(CC(=O)O)c2)cc(C(=O)OC)c1
5-(3,5-bis-(methoxycarbonyl)-phenylazo)-2-hydroxy-phenylacetic acid

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحthe precipitate was filtered off
  2. 2
    workup.ADDITIONwas then diluted with water until a state of weak opalescence
  3. 3
    workup.ADDITIONThe solution was treated with active carbon
  4. 4
    أخرىevaporated down to half its volume
  5. 5
    workup.ADDITIONSodium hydrogen carbonate was added until the solution
  6. 6
    درجة الحرارةThe solution was cooled
  7. 7
    ترشيحthe crystals were filtered off
  8. 8
    أخرىdried

الإجراء التجريبي

20.9 g of dimethyl-5-amino-benzene-1,3-dicarboxylate was dissolved in 20 ml of concentrated hydrochloric acid in 200 ml of ice water. The solution was diazotized with 7 g of sodium nitrite dissolved in 30 ml of water. 30.4 g of 2-hydroxy-phenylacetic acid was dissolved in 200 ml of water and 24 g of sodium hydroxide. The solution was cooled with 100 g of ice. To this hydroxide solution was then added the diazonium salt solution, all at once, and with vigorous stirring. After 30 seconds the solution was acidified with acetic acid and the precipitate was filtered off. The precipitate was leached with an about 25% ethanol solution which was then diluted with water until a state of weak opalescence was reached. The solution was treated with active carbon and evaporated down to half its volume. Sodium hydrogen carbonate was added until the solution was clear, whereupon the solution was heated (80° C.) and acidified with hydrochloric acid. The solution was cooled, the crystals were filtered off and dried.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04725676uspto-grants-1988_02