JPS5484564A - Novel gamma-butyrolactone derivative and its preparation - Google Patents

Novel gamma-butyrolactone derivative and its preparation

Info

Publication number
JPS5484564A
JPS5484564A JP15172177A JP15172177A JPS5484564A JP S5484564 A JPS5484564 A JP S5484564A JP 15172177 A JP15172177 A JP 15172177A JP 15172177 A JP15172177 A JP 15172177A JP S5484564 A JPS5484564 A JP S5484564A
Authority
JP
Japan
Prior art keywords
formula
phenyl
lower alkyl
halogen
group
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.)
Granted
Application number
JP15172177A
Other languages
Japanese (ja)
Other versions
JPS597713B2 (en
Inventor
Yuji Hirose
Katsutoshi Ishikawa
Noboru Iida
Yoshio Nakazawa
Teruhiko Toyama
Hajime Tachibana
Yuji Enomoto
Yasunobu Funakoshi
Takashi Fujita
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP52151721A priority Critical patent/JPS597713B2/en
Publication of JPS5484564A publication Critical patent/JPS5484564A/en
Publication of JPS597713B2 publication Critical patent/JPS597713B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Plural Heterocyclic Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Furan Compounds (AREA)

Abstract

NEW MATERIAL:A γ-butyrolactone derivative of formula I: [A is formula II (R1 is phenyl which is substituted by halogen, naphthyl, furyl, halogen- substituted thienyl group, etc.); formula III (R2 is ≥2C lower alkyl, lower alkenyl, phenyl- carbamoylmethyl group, etc.), formula IV (R3 is ≥2C lower alkyl, phenyl group, etc.; R3' is lower alkyl or phenyl group; R3" and R3"' are H or lower alkyl groups, R3' and R3" or R3"' may form a ring), etc.; Q is H, phenyl or halogen- substituted phenyl group].
EXAMPLE: α-Methylene-γ-phenyl-γ-(2-thienyl)-γ-butyrolactone.
USE: Herbicides and fungicides effective for molds of blast and vegetable pathogenic fungi, e.g. Phizoctonia solani, etc.
PROCESS: A compound of formula II: (A is O) is reacted with a compound of formula V: (R is lower alkyl, Hal is halogen) in the presence of zinc to give the compound of formula I.
COPYRIGHT: (C)1979,JPO&Japio
JP52151721A 1977-12-19 1977-12-19 New γ↓-butyrolactone derivative and its production method Expired JPS597713B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP52151721A JPS597713B2 (en) 1977-12-19 1977-12-19 New γ↓-butyrolactone derivative and its production method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP52151721A JPS597713B2 (en) 1977-12-19 1977-12-19 New γ↓-butyrolactone derivative and its production method

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP13815982A Division JPS58116483A (en) 1982-08-09 1982-08-09 Novel butyrolactone derivative and its preparation

Publications (2)

Publication Number Publication Date
JPS5484564A true JPS5484564A (en) 1979-07-05
JPS597713B2 JPS597713B2 (en) 1984-02-20

Family

ID=15524822

Family Applications (1)

Application Number Title Priority Date Filing Date
JP52151721A Expired JPS597713B2 (en) 1977-12-19 1977-12-19 New γ↓-butyrolactone derivative and its production method

Country Status (1)

Country Link
JP (1) JPS597713B2 (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57211221A (en) * 1981-06-10 1982-12-25 Siemens Ag Method of marking semiconductor chip
JP2006506409A (en) * 2002-11-05 2006-02-23 マグナケム インターナショナル ラボラトリーズ， インコーポレイテッド Synthetic lactone formulations and methods and uses
US8188145B2 (en) 2002-06-12 2012-05-29 Magnachem International Laboratories, Inc. Synthetic lactone formulations and method of use
WO2013047044A1 (en) * 2011-09-29 2013-04-04 Jsr株式会社 Composition for forming film for liquid-immersion exposure, polymer, compound, and method for forming resist pattern
JP2013075964A (en) * 2011-09-29 2013-04-25 Jsr Corp Compound, polymer, and photoresist composition
US8501431B2 (en) 2008-10-24 2013-08-06 Magnachem International Laboratories, Inc. Method for screening for compounds selectively interacting with RAD9
JP2013174669A (en) * 2012-02-23 2013-09-05 Jsr Corp Composition for forming immersion overlay film and method for forming resist pattern
US8536348B2 (en) 2001-06-13 2013-09-17 Magnachem International Laboratories, Inc. Lactone formulations and method of use
CN116217526A (en) * 2023-02-27 2023-06-06 西北农林科技大学 Aromatic heterocyclic substituted α-methylene-γ-butyrolactone compounds, preparation method and application

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6251149U (en) * 1985-09-14 1987-03-30
JPS63186748U (en) * 1987-05-26 1988-11-30
JPS644318U (en) * 1987-06-29 1989-01-11
JPS644317U (en) * 1987-06-29 1989-01-11

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3838168A (en) * 1969-11-21 1974-09-24 Dow Chemical Co Alpha-methylenation of gamma-butyrolactones

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3838168A (en) * 1969-11-21 1974-09-24 Dow Chemical Co Alpha-methylenation of gamma-butyrolactones

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57211221A (en) * 1981-06-10 1982-12-25 Siemens Ag Method of marking semiconductor chip
US8536348B2 (en) 2001-06-13 2013-09-17 Magnachem International Laboratories, Inc. Lactone formulations and method of use
US8188145B2 (en) 2002-06-12 2012-05-29 Magnachem International Laboratories, Inc. Synthetic lactone formulations and method of use
JP2006506409A (en) * 2002-11-05 2006-02-23 マグナケム インターナショナル ラボラトリーズ， インコーポレイテッド Synthetic lactone formulations and methods and uses
US7956088B2 (en) 2002-11-05 2011-06-07 Magnachem International Laboratories, Inc. Synthetic lactone formulations and methods of use
JP4869597B2 (en) * 2002-11-05 2012-02-08 マグナケム インターナショナル ラボラトリーズ， インコーポレイテッド Synthetic lactone formulations and methods of use
US8546444B2 (en) 2004-04-23 2013-10-01 Magnachem International Laboratories, Inc. Synthetic lactone formulations and method of use
US8501431B2 (en) 2008-10-24 2013-08-06 Magnachem International Laboratories, Inc. Method for screening for compounds selectively interacting with RAD9
WO2013047044A1 (en) * 2011-09-29 2013-04-04 Jsr株式会社 Composition for forming film for liquid-immersion exposure, polymer, compound, and method for forming resist pattern
JP2013075964A (en) * 2011-09-29 2013-04-25 Jsr Corp Compound, polymer, and photoresist composition
JP2013174669A (en) * 2012-02-23 2013-09-05 Jsr Corp Composition for forming immersion overlay film and method for forming resist pattern
CN116217526A (en) * 2023-02-27 2023-06-06 西北农林科技大学 Aromatic heterocyclic substituted α-methylene-γ-butyrolactone compounds, preparation method and application

Also Published As

Publication number Publication date
JPS597713B2 (en) 1984-02-20

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