Reaktion #1435683

ord-1218509bf7364d2ebeac4cecb4929ad8

Reaktionsgleichung

COc1c(C)cc(N)cc1N.Cl.Cl
2,4-diamino-6-methylanisole dihydrochloride
O=C([O-])[O-].[Ca+2]
calcium carbonate
C1COCCO1
dioxane
O=C(Cl)OCCCl
2-chloroethyl chloroformate
COc1c(C)cc(NC(=O)OCCCl)cc1NC(=O)OCCCl
Bis(2-chloroethyl) (4-methoxy-5-methyl-1,3-phenylene)biscarbamate

Reaktionsbedingungen

Temperatur
90°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.WAITSubsequently, the mixture was left
  2. 2
    Temperaturto cool
  3. 3
    Filtrationthe mineral salts were filtered off
  4. 4
    workup.ADDITIONThe filtrate was poured onto iced water
  5. 5
    Extraktionthe mixture was extracted several times with ethyl acetate
  6. 6
    SonstigeThe combined ethyl acetate phases were then evaporated to dryness on a Rotavapor
  7. 7
    Sonstigegiving pale brown crystals

Vorschrift

56 g of 2,4-diamino-6-methylanisole dihydrochloride and 134 g of calcium carbonate were initially introduced into 1 l of dioxane and heated to 90° C. Within 15 min, 80 g of 2-chloroethyl chloroformate were added and the mixture was stirred for a further 4 h at this temperature. Subsequently, the mixture was left to cool, and the mineral salts were filtered off. The filtrate was poured onto iced water, and the mixture was extracted several times with ethyl acetate. The combined ethyl acetate phases were then evaporated to dryness on a Rotavapor, giving pale brown crystals.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07211119B2uspto-grants-2007_05