JPS54145653A - Dihalophenyl 1-pyrrolidine-carbodithioate - Google Patents

Dihalophenyl 1-pyrrolidine-carbodithioate

Info

Publication number
JPS54145653A
JPS54145653A JP5348278A JP5348278A JPS54145653A JP S54145653 A JPS54145653 A JP S54145653A JP 5348278 A JP5348278 A JP 5348278A JP 5348278 A JP5348278 A JP 5348278A JP S54145653 A JPS54145653 A JP S54145653A
Authority
JP
Japan
Prior art keywords
formula
compound
pyrrolidine
reacted
solvent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP5348278A
Other languages
Japanese (ja)
Inventor
Tetsuo Takematsu
Masato Konnai
Takuji Nishida
Takeo Hosogai
Masao Mizuno
Michihiro Ishiguro
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kuraray Co Ltd
Original Assignee
Kuraray Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kuraray Co Ltd filed Critical Kuraray Co Ltd
Priority to JP5348278A priority Critical patent/JPS54145653A/en
Publication of JPS54145653A publication Critical patent/JPS54145653A/en
Pending legal-status Critical Current

Links

Abstract

NEW MATERIAL:A compound of formula I: (Two X's are halogens).
USE: Paddy field herbicides having improved control effects on broadleaf weeds, and little damage to rice plants, showing the best effect within the second leaf period after germination of weeds.
PROCESS: The compound is prepared by the following four methods: (1) A com- pound of formula II is reacted with pyrrolidine of formula III in the presence of a base, e.g. trimethylamine or pyridine, at-50 to 100°C. (2) The reaction is carried out under the same conditions as in (1) except that pyrrolidine connot be used as a base. (3) A compoud of formula IV is reacted with a compound of formula V in a solvent at-50 to 100°C. (4) A compound of formula VI: (X is formula I is reacted with a compound of formula VII in a solvent at 30 to 300°C. Diethyl ether, THF, or benzene may be cited as the solvent.
COPYRIGHT: (C)1979,JPO&Japio
JP5348278A 1978-05-04 1978-05-04 Dihalophenyl 1-pyrrolidine-carbodithioate Pending JPS54145653A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5348278A JPS54145653A (en) 1978-05-04 1978-05-04 Dihalophenyl 1-pyrrolidine-carbodithioate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5348278A JPS54145653A (en) 1978-05-04 1978-05-04 Dihalophenyl 1-pyrrolidine-carbodithioate

Publications (1)

Publication Number Publication Date
JPS54145653A true JPS54145653A (en) 1979-11-14

Family

ID=12944050

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5348278A Pending JPS54145653A (en) 1978-05-04 1978-05-04 Dihalophenyl 1-pyrrolidine-carbodithioate

Country Status (1)

Country Link
JP (1) JPS54145653A (en)

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