Реакция #4408

ord-adafda2f10aa459986df317fa2d32be6

Уравнение реакции

N#CCCl
chloroacetonitrile
COc1ccc2[nH]ccc2c1
5-methoxyindole
NC(N)=S
thiourea
II
I2
COc1ccc2[nH]cc(SCC#N)c2c1
5-methoxy-3-cyanomethylthioindole
Выход 42.0%

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe reaction mixture was then evaporated in vacuo to about 1100 ml, 68 ml of 50% aqueous NaOH
  2. 2
    workup.ADDITIONwere added under nitrogen
  3. 3
    Другоеbrought to 85°
  4. 4
    workup.STIRRINGthe mixture was stirred at 80°-90° for 40 minutes
  5. 5
    ТемператураThe mixture was cooled
  6. 6
    Фильтрацияfiltered through glass wool and under nitrogen
  7. 7
    workup.WAITto proceed under N2 for 18 hours
  8. 8
    Другоеthe ether was separated off
  9. 9
    workup.DISSOLUTIONhaving dissolved a large portion of suspended solid material
  10. 10
    ЭкстракцияThe aqueous solution was extracted three times with 500 ml portions of ether which
  11. 11
    Сушкаdried over anhydrous K2CO3
  12. 12
    ФильтрацияThe ether layer was filtered

Методика

To a solution of 50 g (0.34 mole) of 5-methoxyindole and 25.8 (0.34 mole) of thiourea in 1700 ml of 50% aqueous methanol was added 340 ml of KI/I2 in water over a 5 minute period and the reaction mixture was allowed to stir at room temperature for 3 hours. The reaction mixture was then evaporated in vacuo to about 1100 ml, 68 ml of 50% aqueous NaOH were added under nitrogen, the temperature brought to 85° and the mixture was stirred at 80°-90° for 40 minutes. The mixture was cooled and filtered through glass wool and under nitrogen, 21.2 ml (25.4 g; 0.34 mole) of chloroacetonitrile were added. The reaction was allowed to proceed under N2 for 18 hours after which the reaction mixture was layered over with about 800 ml of diethyl ether and the ether was separated off having dissolved a large portion of suspended solid material. The aqueous solution was extracted three times with 500 ml portions of ether which were combined with the other washings and dried over anhydrous K2CO3. The ether layer was filtered and evaporated in vacuo to 33 g of 5-methoxy-3-cyanomethylthioindole (42% yield) as a tan solid.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04725604uspto-grants-1988_02