JPS6485950A - Diethyl aromatic compound and production thereof - Google Patents

Diethyl aromatic compound and production thereof

Info

Publication number
JPS6485950A
JPS6485950A JP62266068A JP26606887A JPS6485950A JP S6485950 A JPS6485950 A JP S6485950A JP 62266068 A JP62266068 A JP 62266068A JP 26606887 A JP26606887 A JP 26606887A JP S6485950 A JPS6485950 A JP S6485950A
Authority
JP
Japan
Prior art keywords
substituted
formula
aromatic compound
production
hydrocarbon 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
JP62266068A
Other languages
Japanese (ja)
Other versions
JP2529299B2 (en
Inventor
Tomoyuki Shimada
Masaomi Sasaki
Mitsuru Hashimoto
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.)
Ricoh Co Ltd
Original Assignee
Ricoh 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 Ricoh Co Ltd filed Critical Ricoh Co Ltd
Priority to JP62266068A priority Critical patent/JP2529299B2/en
Priority to US07/171,422 priority patent/US4886846A/en
Priority to DE3810522A priority patent/DE3810522C2/en
Publication of JPS6485950A publication Critical patent/JPS6485950A/en
Priority to US07/642,686 priority patent/US5159087A/en
Priority to US07/838,672 priority patent/US5250377A/en
Application granted granted Critical
Publication of JP2529299B2 publication Critical patent/JP2529299B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G03G5/0601—Acyclic or carbocyclic compounds
    • G03G5/0612—Acyclic or carbocyclic compounds containing nitrogen
    • G03G5/0614—Amines
    • G03G5/06142—Amines arylamine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/86—Benzo [b] furans; Hydrogenated benzo [b] furans with an oxygen atom directly attached in position 7
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/30—Hetero atoms other than halogen
    • C07D333/36—Nitrogen atoms
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G03G5/0622—Heterocyclic compounds
    • G03G5/0624—Heterocyclic compounds containing one hetero ring
    • G03G5/0627—Heterocyclic compounds containing one hetero ring being five-membered
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G03G5/0622—Heterocyclic compounds
    • G03G5/0644—Heterocyclic compounds containing two or more hetero rings
    • G03G5/0661—Heterocyclic compounds containing two or more hetero rings in different ring systems, each system containing at least one hetero ring

Abstract

NEW MATERIAL:A diethyl aromatic compound expressed by formula I [Ar is (substituted) aromatic hydrocarbon group; A is N-substituted carbazolyl or formula II; Ar' is (substituted) aromatic hydrocarbon group; R<1> and R<2> are (substituted) alkyl or (substituted) aryl]. EXAMPLE:1,4-Bis[2-(4-N,N-diphenylaminophenyl)ethyl]benzene. USE:Useful as an organic photoconductive material for electrophotography. PREPARATION:An olefin expressed by formula III is reduced to provide the aimed compound expressed by formula I. The reduction is carried out in the presence of a metallic salt, metallic hydride compound or catalyst for catalytic hydrogenation in a solvent, such as dioxane.
JP62266068A 1987-03-28 1987-10-20 Diethyl aromatic compound and method for producing the same Expired - Lifetime JP2529299B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP62266068A JP2529299B2 (en) 1987-04-21 1987-10-20 Diethyl aromatic compound and method for producing the same
US07/171,422 US4886846A (en) 1987-03-28 1988-03-21 Aromatic diolefinic compounds, aromatic diethyl compounds and electrophotographic photoconductors comprising one aromatic diethyl compound
DE3810522A DE3810522C2 (en) 1987-03-28 1988-03-28 Aromatic diethyl compounds and electrophotographic photoconductors containing an aromatic diethyl compound
US07/642,686 US5159087A (en) 1987-03-28 1991-01-17 Aromatic diolefinic compounds, aromatic diethyl compounds and electrophotographic photoconductors comprising one aromatic diethyl compound
US07/838,672 US5250377A (en) 1987-03-28 1992-02-21 Aromatic diolefinic compounds, aromatic diethyl compounds and electrophotographic photoconductors comprising one aromatic diethyl compound

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP62-98393 1987-04-21
JP9839387 1987-04-21
JP62-142178 1987-06-09
JP14217887 1987-06-09
JP62266068A JP2529299B2 (en) 1987-04-21 1987-10-20 Diethyl aromatic compound and method for producing the same

Publications (2)

Publication Number Publication Date
JPS6485950A true JPS6485950A (en) 1989-03-30
JP2529299B2 JP2529299B2 (en) 1996-08-28

Family

ID=27308661

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62266068A Expired - Lifetime JP2529299B2 (en) 1987-03-28 1987-10-20 Diethyl aromatic compound and method for producing the same

Country Status (1)

Country Link
JP (1) JP2529299B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007233425A (en) * 2002-12-05 2007-09-13 Ricoh Co Ltd Photoreceptor, image forming method using same, image forming apparatus, and process cartridge for image forming apparatus

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002014478A (en) 2000-06-30 2002-01-18 Hodogaya Chem Co Ltd Method for refining material of electronic product

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007233425A (en) * 2002-12-05 2007-09-13 Ricoh Co Ltd Photoreceptor, image forming method using same, image forming apparatus, and process cartridge for image forming apparatus

Also Published As

Publication number Publication date
JP2529299B2 (en) 1996-08-28

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