تفاعل #55727

ord-3e5bf0f31f17404389ba2da23fd2371d

معادلة التفاعل

Cl
hyrochloric acid
Nc1ccc(I)cc1C(=O)O
5-iodoanthranilic acid
[Na+].[OH-]
sodium hydroxide
O=N[O-].[Na+]
sodium nitrite
Cl
hydrochloric acid
CCOC(=S)[S-].[K+]
potassium ethyl xanthate
O=N[O-]
nitrite
[Na+].[OH-]
sodium hydroxide
CC(=O)[O-].[K+]
potassium acetate
O=C(O)c1cc(I)ccc1S
5-iodothiosalicyclic acid
المردود 80.5%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas maintained between 0° and 5°
  2. 2
    درجة الحرارةby external cooling and by the addition of ice
  3. 3
    أخرىpreheated to 75°-80°
  4. 4
    درجة الحرارةthe reaction mixture was cooled
  5. 5
    أخرىAfter decanting the aqueous phase
  6. 6
    workup.DISSOLUTIONthe resulting sludge was dissolved in 10 percent sodium hydroxide solution (200 ml)
  7. 7
    درجة الحرارةheated on a steam bath for two hours
  8. 8
    درجة الحرارةThe solution was cooled
  9. 9
    ترشيحfiltered
  10. 10
    أخرىthe solid collected
  11. 11
    غسيلwashed
  12. 12
    أخرىdried
  13. 13
    درجة الحرارةThe resulting disulfide was refluxed for 16 hours with zinc dust (25 g) in glacial acetic acid (750 ml)
  14. 14
    أخرىThe solid was collected
  15. 15
    غسيلwashed with cold water
  16. 16
    workup.WAITdigested with concentrated hydrochloric acid for 30 minutes
  17. 17
    ترشيحfiltered
  18. 18
    غسيلwashed with water
  19. 19
    أخرىdried

الإجراء التجريبي

A solution of 5-iodoanthranilic acid (71.1 g; 0.272 mole), sodium hydroxide (11.5 g; 0.275 mole) and sodium nitrite (18.75 g; 0.275 mole) in water (325 ml) was added slowly with stirring to a mixture of concentrated hydrochloric acid (75 ml) and ice (100 g) while the temperature was maintained between 0° and 5° by external cooling and by the addition of ice. After completion of the addition of the nitrite solution, the mixture was stirred for an additional 30 minutes and adjusted to pH 7 with dilute sodium hydroxide solution and potassium acetate. The cold diazonium mixture was added to a vigorously stirred solution of potassium ethyl xanthate (125 g; 0.775 mole) in water (400 ml) preheated to 75°-80°. When the evolution of nitrogen ceased, the reaction mixture was cooled and acidified to pH 3 with concentrated hyrochloric acid. After decanting the aqueous phase, the resulting sludge was dissolved in 10 percent sodium hydroxide solution (200 ml) and heated on a steam bath for two hours. The solution was cooled, filtered, acidified to pH 4-5 with concentrated hydrochloric acid, and the solid collected, washed and dried. The resulting disulfide was refluxed for 16 hours with zinc dust (25 g) in glacial acetic acid (750 ml). The solid was collected, washed with cold water, digested with concentrated hydrochloric acid for 30 minutes, filtered, washed with water and dried to give 5-iodothiosalicyclic acid (61.3 g), m.p. 208°-210°. Treatment of 5-iodothiosalicyclic acid (60 g) with acetic anhydride (300 ml) and concentrated sulfuric acid (1 ml) at 100° for one hour yielded 5-iodoacetylthiosalicylic acid (35.1 g), m.p. 163°14 165°.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04221800uspto-grants-1980_09