Реакция #312358

ord-1ce20f5aa28a4ada85c0362ed2b20f85

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGthe reaction mixture was stirred vigorously for an additional 5 mins
  2. 2
    workup.WAITThe reaction mixture was left
  3. 3
    workup.WAITstanding at room temperature for 10 mins
  4. 4
    workup.WAIT, then it was placed in an ice-bath for 0.5 hr
  5. 5
    ДругоеThe crystals which formed
  6. 6
    Другоеwere collected
  7. 7
    Промывкаwashed with 95% ethanol and air
  8. 8
    Другоеdried
  9. 9
    ДругоеRecrystallization from 85% ethanol

Методика

o-Chlorobenzaldehyde (0.20 mole) was treated with 3-chloro-2-methylaniline (0.20 mole) with vigorous stirring in a 1 liter Erlenmeyer Flask. After 15 mins., 33 cc of 95% ethanol was added and the reaction mixture was stirred vigorously for an additional 5 mins. The reaction mixture was left standing at room temperature for 10 mins., then it was placed in an ice-bath for 0.5 hr. The crystals which formed were collected, washed with 95% ethanol and air dried. Recrystallization from 85% ethanol gave N-(o-chlorobenzylidene)-3-chloro-2-methylaniline. m.p. 83°-85° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04235929uspto-grants-1980_11