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[ CAS No. 86014-80-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 86014-80-4
Chemical Structure| 86014-80-4
Structure of 86014-80-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 86014-80-4 ]

CAS No. :86014-80-4 MDL No. :MFCD09673407
Formula : C8H15Cl2N Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 196.12 Pubchem ID :-
Synonyms :

Safety of [ 86014-80-4 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 86014-80-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 86014-80-4 ]

[ 86014-80-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 92-84-2 ]
  • [ 86014-80-4 ]
  • [ 87-69-4 ]
  • [ 29216-28-2 ]
YieldReaction ConditionsOperation in experiment
In 5,5-dimethyl-1,3-cyclohexadiene; acetic acid methyl ester; water; ethyl acetate 2 10-(3-Quinuclidinyl-methyl)-phenothiazine SPC9 EXAMPLE 2 10-(3-Quinuclidinyl-methyl)-phenothiazine SPC9 30 g of phenothiazine were added, all at once, to a suspension of 6 g of sodium amide in 240 ml of anhydrous xylene. The mixture was agitated and heated to reflux. When evolution of ammonia ceased (5 hours), 15 g of 3-chloromethyl-quinuclidine hydrochloride were added portionwise over a period of 50 minutes and reflux was then maintained for 22 hours. After cooling to room temperature, 250 ml of distilled water and 250 ml of ethyl acetate were added to the reaction mixture. The aqueous phase was decanted and extracted twice with a total of 250 ml of methyl acetate. The combined organic extracts were extracted three times with a total of 750 ml of a 10% aqueous solution of tartaric acid. The combined acid solutions were treated with 5 g of animal charcoal, filtered and rendered alkaline on an ice bath with 96 ml of ION aqueous caustic soda. The oil which separated was extracted three times with a total of 1500 ml of ethyl acetate. The combined organic extracts were washed to neutrality by washing twice with a total of 1 l. of distilled water, dried over anhydrous magnesium sulphate and evaporated under reduced pressure on a water bath at 45° C. 17 g of oil were obtained which was purified by chromatography on an inert alumina column as in Example 1. 13.3 g of crystallized product were obtained. 10-(3-Quinuclidinyl-methyl)-phenothiazine having m.p. 130° - 131° C was obtained by recrystallisation in boiling acetonitrile.
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