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JPS56115774A - N-substituted-3-alkenyl-6-halocarbazole and its preparation - Google Patents

N-substituted-3-alkenyl-6-halocarbazole and its preparation

Info

Publication number
JPS56115774A
JPS56115774A JP1853280A JP1853280A JPS56115774A JP S56115774 A JPS56115774 A JP S56115774A JP 1853280 A JP1853280 A JP 1853280A JP 1853280 A JP1853280 A JP 1853280A JP S56115774 A JPS56115774 A JP S56115774A
Authority
JP
Japan
Prior art keywords
halocarbazole
substituted
alkenyl
formula
formyl
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
JP1853280A
Other languages
Japanese (ja)
Other versions
JPH0215536B2 (en
Inventor
Hiroshi Kawahara
Iwahiro Otsuka
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.)
AGC Inc
Original Assignee
Asahi Glass 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 Asahi Glass Co Ltd filed Critical Asahi Glass Co Ltd
Priority to JP1853280A priority Critical patent/JPS56115774A/en
Publication of JPS56115774A publication Critical patent/JPS56115774A/en
Publication of JPH0215536B2 publication Critical patent/JPH0215536B2/ja
Granted legal-status Critical Current

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  • Indole Compounds (AREA)

Abstract

NEW MATERIAL:An N-substituted -3-alkenyl-6-halocarbazole expressed by formula I (R is 1W16C alkyl, alkyloxyalkyl or aralkyl; R1 and R2 are H or CH3; X is Br or I).
EXAMPLE: 3-Bromo-6-vinyl-9-n-dodecylcarbazole.
USE: A synthetic intermediate for a photoconductive material or a monomer for preparing a conjugated polymer to be a photoconductive material. Useful as a photosensitive material for electrophotography.
PROCESS: The formyl group or acetyl group of an N-substituted -3-formyl(or acetyl)- 6-halocarbazole expressed by formula II (Y is formyl or acetyl) is reacted with methylenephosphorane or ethylidenephosphorane generated from a phosphonium salt under anhydrous or phase transfer conditions and converted into an alkenyl group and give the compound of formula I.
COPYRIGHT: (C)1981,JPO&Japio
JP1853280A 1980-02-19 1980-02-19 N-substituted-3-alkenyl-6-halocarbazole and its preparation Granted JPS56115774A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1853280A JPS56115774A (en) 1980-02-19 1980-02-19 N-substituted-3-alkenyl-6-halocarbazole and its preparation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1853280A JPS56115774A (en) 1980-02-19 1980-02-19 N-substituted-3-alkenyl-6-halocarbazole and its preparation

Publications (2)

Publication Number Publication Date
JPS56115774A true JPS56115774A (en) 1981-09-11
JPH0215536B2 JPH0215536B2 (en) 1990-04-12

Family

ID=11974230

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1853280A Granted JPS56115774A (en) 1980-02-19 1980-02-19 N-substituted-3-alkenyl-6-halocarbazole and its preparation

Country Status (1)

Country Link
JP (1) JPS56115774A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003050086A1 (en) * 2001-12-12 2003-06-19 The University Of Sheffield 2, 7 - substituted carbazoles and oligomers, polymers and co-polymers thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003050086A1 (en) * 2001-12-12 2003-06-19 The University Of Sheffield 2, 7 - substituted carbazoles and oligomers, polymers and co-polymers thereof

Also Published As

Publication number Publication date
JPH0215536B2 (en) 1990-04-12

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