تفاعل #78210

ord-5698eedece90432c9b83a625bb4512b2

معادلة التفاعل

CCN(CC)CC
triethylamine
Nc1ccc(Br)c2ccccc12
1-amino-4-bromonaphthalene
[Na+].[OH-]
sodium hydroxide
COC(=O)c1ccc(N)c2ccccc12
methyl 4-amino-1-naphthalenecarboxylate
Nc1ccc(C(=O)O)c2ccccc12
title compound
Nc1ccc(C(=O)O)c2ccccc12
4-Amino-1-naphthalenecarboxylic acid

ظروف التفاعل

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

المعالجة

  1. 1
    تركيزAfter the concentration under reduced pressure, water
  2. 2
    workup.ADDITIONwas added to the reaction mixture
  3. 3
    استخلاصthe product was extracted with ethyl acetate
  4. 4
    تركيزconcentrated
  5. 5
    أخرىthus obtained
  6. 6
    أخرىEthanol was evaporated
  7. 7
    غسيلthe residue was washed with ethyl acetate
  8. 8
    استخلاصAfter the extraction with ethyl acetate
  9. 9
    غسيلthe product was washed with water and saturated aqueous sodium chloride solution
  10. 10
    تجفيفdried over anhydrous sodium sulfate
  11. 11
    تركيزconcentrated under reduced pressure

الإجراء التجريبي

1.60 g (2.3 mmol) of bis(triphenylphosphine)dichloropalladium, 7.0 ml (50.6 mmol) of triethylamine and 60 ml of methanol were successively added to a mixture of 5.00 g (22.5 mmol) of 1-amino-4-bromonaphthalene and 60 ml of dimethylformamide, and they were stirred in carbon monoxide atmosphere at 80° C. for 2 days. After the concentration under reduced pressure, water was added to the reaction mixture and the product was extracted with ethyl acetate and concentrated. 20 ml of ethanol and 10 ml (40.0 mmol) of 4 N aqueous sodium hydroxide solution were added to crude methyl 4-amino-1-naphthalenecarboxylate thus obtained. They were stirred at 80° C. overnight. Ethanol was evaporated, and the residue was washed with ethyl acetate. The aqueous layer was neutralized with hydrochloric acid. After the extraction with ethyl acetate, the product was washed with water and saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain the title compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06710056B2uspto-grants-2004_03