Utilisation du di-(p-chlorophényl)-cyclopropyl-méthanol comme arachnicide et fongicide

1,147,523. Chlorophenyl substituted methanol. JANSSEN PHARMACEUTICA N.V. 19 July, 1966 [29 July, 1965; 18 May, 1966], No. 32393/66. Heading C2C. [Also in Division A5] Di - (p - chlorophenyl) - cyclopropyl - methanol is prepared by reacting 4-chlorophenylcyclopropylketone and 4-chlorophenyl-magnesium...

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Bibliographic Details
Main Authors CORNEEL ROEVENS,LEOPOLD FRANS, FLORENT BUSSCHOTS,ARMAND AUGUST
Format Patent
LanguageFrench
Published 28.02.1969
Edition1
Subjects
ACYCLIC OR CARBOCYCLIC COMPOUNDS
ARTIFICIAL STONE
CASTING
CEMENTS
CERAMICS
CHEMISTRY
COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDINGMATERIALS
CONCRETE
FOUNDRY MOULDING
LIME, MAGNESIA
METALLURGY
ORGANIC CHEMISTRY
PERFORMING OPERATIONS
POWDER METALLURGY
REFRACTORIES
SLAG
TRANSPORTING
TREATMENT OF NATURAL STONE
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Summary:1,147,523. Chlorophenyl substituted methanol. JANSSEN PHARMACEUTICA N.V. 19 July, 1966 [29 July, 1965; 18 May, 1966], No. 32393/66. Heading C2C. [Also in Division A5] Di - (p - chlorophenyl) - cyclopropyl - methanol is prepared by reacting 4-chlorophenylcyclopropylketone and 4-chlorophenyl-magnesium chloride in tetrahydrofuran and xylene. The 4-chlorophenyl-cyclopropyl ketone is prepared by reacting potassium hydroxide and 4 - chloro - 41 - chlorobutyrophenone; the latter compound being obtained by heating butyrolactone and thionyl chloride in the presence of zinc chloride and then reacting the resulting 4-chlorobutyryl chloride with excess chlorobenzene.
Bibliography:Application Number: CH19660010109