Реакция #459743

ord-49afc5362aa240438ceb1d48d91fa22a

Растворители

Условия реакции

Температура
20°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe mixture was refluxed for 20 minutes
  2. 2
    ЭкстракцияThe mixture was extracted with methylene chloride
  3. 3
    Промывкаthe organic extracts were washed with water
  4. 4
    Другоеdried
  5. 5
    Другоеevaporated to dryness
  6. 6
    workup.DISSOLUTIONThe resulting 3.5 g of product were dissolved in 5 ml of ethyl acetate
  7. 7
    workup.ADDITIONa solution of ethyl acetate saturated with hydrogen chloride was added
  8. 8
    Другоеat 10° C
  9. 9
    Фильтрацияfiltered

Методика

7.4 ml of concentrated sulfuric acid were added to a refluxing solution of 3.7 g of 3-chloro-5ξ-hydroxy-7-methylamino-6,7,8,9-tetrahydro [5H] benzocycloheptene in 37 ml of dioxane and the mixture was refluxed for 20 minutes and then was cooled to 20° C. 50 ml of water were added to the reaction mixture which was then made alkaline with sodium hydroxide. The mixture was extracted with methylene chloride and the organic extracts were washed with water, dried and evaporated to dryness. The resulting 3.5 g of product were dissolved in 5 ml of ethyl acetate and a solution of ethyl acetate saturated with hydrogen chloride was added thereto at 10° C. The mixture was vacuum filtered to obtain 3.3 g of 2-chloro-7-methylamino-6,7-dihydro [5H] benzocycloheptene hydrochloride melting at 195° C which was identical to the product of Example 10.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04091115uspto-grants-1978_05