Sankyo Company, Limited

Takuo Konotsune

Katsuhiko Kawakubo

Junzo Tobitsuka

Takashi Matsui

An ester of a compound having the formula ##STR1## wherein R.sub.1 represents hydrogen atom or a lower alkyl group,

Organic acid esters of 4-benzoyl-5-hydroxy(mercapto)pyrazoles

Herbicidally active compound having the formula ##STR1## wherein R.sub.1 represents hydrogen atom or a lower alkyl group,

Herbicidal 4-benzoyl-5-hydroxy-pyrazales

Herbicidal compositions and pyrazole derivatives

Herbicidal compositions containing as an active ingredient one or more of the pyrazole compounds having the formula ##STR1## (wherein R.sub.1 represents hydrogen atom or a lower alkyl group, R.sub.2 represents a lower alkyl group or a lower alkenyl group, X represents a halogen atom, nitro group, a lower alkyl group, a halogenated lower alkyl group, a lower alkoxy group, a lower alkanesulfonyl group, cyano group, a lower alkylthio group or an aliphatic acyl group and n is an integer of 1 to 4 and when n is 2, 3 or 4, X's may be the same or different), salts thereof and organic acid esters thereof, as well as new pyrazole compounds having herbicidal activities and the formula ##STR2## (wherein R.sub.1 represents hydrogen atom or a lower alkyl group, R.sub.2 represents a lower alkyl group or a lower alkenyl group Z represents a halogen atom, nitro group, a lower alkyl group, a halogenated lower alkyl group, a lower alkoxy group, a lower alkanesulfonyl group, cyano group, a lower alkylthio group, an aliphatic acyl group or benzoyl group, n is an integer of 1 to 4, when n is 2,3 or 4, Z's may be the same or different and Y represents oxygen atom or sulfur atom; provided that those wherein R.sub.1 and R.sub.2 are methyl groups, Z is chlorine atom at 2-position, n is 1 and Y is oxygen atom and wherein R.sub.1 and R.sub.2 are methyl groups, Z is nitro group at 4-position, n is 1 and Y is oxygen atom are excluded. These pyrazole compounds are prepared in a conventional manner.

Herbicidal compositions containing as on active ingredient one or more of the pyrazole compounds having the formula ##STR1## (wherein R.sub.1 represents hydrogen atom or a lower alkyl group, R.sub.2 represents a lower alkyl group or a lower alkenyl group, X represents a halogen atom, nitro group, a lower alkyl group, a halogenated lower alkyl group, a lower alkyl group, a lower alkanesulfonyl group, cyano group, a lower alkylthio group or an aliphatic acyl group and n is an integer of 1 to 4 and when n is 2, 3 or 4, X's may be the same or different), salts thereof and organic acid esters thereof, as well as new pyrazole compounds having herbicidal activities and the formula ##STR2## (wherein R.sub.1 represents hydrogen atom or a lower alkyl group, R.sub.2 represents a lower alkyl group or a lower alkenyl group Z represents a halogen atom, nitro group, a lower alkyl group, a halogenated lower alkyl group, a lower alkoxy group, a lower alkanesulfonyl group, cyano group, a lower alkylthio group, an aliphatic acyl group or benzoyl group, n is an integer of 1 to 4, when n is 2, 3 or 4, Z's may be the same or different and Y represents oxygen atom or sulfur atom; provided that those wherein R.sub.1 and R.sub.2 are methyl groups, Z is chlorine atom at 2-position, n is 1 and Y is oxygen atom and wherein R.sub.1 and R.sub.2 are methyl groups, Z is nitro group at 4-position, n is 1 and Y is oxygen atom are excluded. These pyrazole compounds are prepared in a conventional manner.

Herbicidal compositions containing as an active ingredient one or more of the pyrazole compounds having the formula ##STR1## (wherein R.sub.1 represents hydrogen atom or a lower alkyl group, R.sub.2 represents a lower alkyl group or a lower alkenyl group, X represents a halogen atom, nitro group, a lower alkyl group, a halogenated lower alkyl group, a lower alkoxy group, a lower alkanesulfonyl group, cyano group, a lower alkylthio group or an aliphatic acyl group and n is an integer of 1 to 4 and when n is 2, 3 or 4, X's may be the same or different), salts thereof and organic acid esters thereof, as well as new pyrazole compounds having herbicidal activities and the formula ##STR2## (wherein R.sub.1 represents hydrogen atom or a lower alkyl group, R.sub.2 represents a lower alkyl group or a lower alkenyl group Z represents a halogen atom, nitro group, a lower alkyl group, a halogenated lower alkyl group, a lower alkoxy group, a lower alkanesulfonyl group, cyano group, a lower alkylthio group, an aliphatic acyl group or benzoyl group, n is an integer of 1 to 4, when n is 2, 3 or 4, Z's may be the same or different and Y represents oxygen atom or sulfur atom); provided that those wherein R.sub.1 and R.sub.2 are methyl groups, Z is chlorine atom at 2-position, n is 1 and Y is oxygen atom and wherein R.sub.1 and R.sub.2 are methyl groups, Z is nitro group at 4-position, n is 1 and Y is oxygen atom are excluded. These pyrazole compounds are prepared in a conventional manner.

Pyrazole sulfonates

4-Benzoyl-5-hydroxypyrazole derivatives are prepared by treating 5-benzoyloxypyrazole derivatives with more than 1 equivalent mole of alkaline substance or more than 1 mole of aluminum chloride per mole of the 5-benzoyloxypyrazole derivatives. The desired pyrazole derivatives are useful as a herbicide.

Process for the preparation of 4-benzoylpyrazole derivatives

Herbicidal compositions

Pyrazolone compounds of the formula ##STR1## WHEREIN R.sub.1 represents a hydrogen atom or a lower alkyl group, R.sub.2 represents a lower alkyl group or a lower alkenyl group, X represents a halogen atom, Y represents a halogen atom, a nitro group, a lower alkyl group or a lower alkoxy group, n is an integer of 1 to 3 and when n is 2 or 3, Y's may be the same or different. These compounds are useful as herbicides and obtainable by reacting the corresponding 5-pyrazolone derivatives with a halogenating agent.

Growing community of inventors

Hiromachi, Japan

Takuo Konotsune