JPS57185248A - Preparation of benzenediazonium sulfate - Google Patents

Preparation of benzenediazonium sulfate

Info

Publication number
JPS57185248A
JPS57185248A JP7110281A JP7110281A JPS57185248A JP S57185248 A JPS57185248 A JP S57185248A JP 7110281 A JP7110281 A JP 7110281A JP 7110281 A JP7110281 A JP 7110281A JP S57185248 A JPS57185248 A JP S57185248A
Authority
JP
Japan
Prior art keywords
aniline sulfate
sulfate
reaction
give
diazotation
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
JP7110281A
Other languages
Japanese (ja)
Inventor
Shigeo Wake
Tetsuo Murata
Yoshihide Mori
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP7110281A priority Critical patent/JPS57185248A/en
Publication of JPS57185248A publication Critical patent/JPS57185248A/en
Pending legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PURPOSE: To obtain the titled compound in high yield, by reacting an aqueous slurry solution of aniline sulfate with nitrogen oxide while controlling the feed rates of both to give the concentration of the aniline sulfate in the aqueous medium at a specific standard or below always.
CONSTITUTION: Aniline sulfate is reacted with a mixture of nitrogen oxides, e.g. NO, NO2 or N2O3, in an aqueous medium to prepare benzenediazonium sulfate. In the process, the feed rates of the raw materials are controlled to give the concentration of the aniline sulfate in the reaction medium of 8wt% or below always, and the diazotation reaction is carried out substantially in the absence of the aniline sulfate slurry in the reaction medium to give the aimed compound. The aniline sulfate fed to the reaction system is converted into the aimed soluble compound in the aqueous medium without accumulating therein. Thus, the diazotation proceeds smoothly due to no deposition of a solid. The diazotation reaction temperature is -10W+10°C, preferably -5W+3°C.
COPYRIGHT: (C)1982,JPO&Japio
JP7110281A 1981-05-11 1981-05-11 Preparation of benzenediazonium sulfate Pending JPS57185248A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7110281A JPS57185248A (en) 1981-05-11 1981-05-11 Preparation of benzenediazonium sulfate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7110281A JPS57185248A (en) 1981-05-11 1981-05-11 Preparation of benzenediazonium sulfate

Publications (1)

Publication Number Publication Date
JPS57185248A true JPS57185248A (en) 1982-11-15

Family

ID=13450840

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7110281A Pending JPS57185248A (en) 1981-05-11 1981-05-11 Preparation of benzenediazonium sulfate

Country Status (1)

Country Link
JP (1) JPS57185248A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS615061A (en) * 1984-06-15 1986-01-10 Sumitomo Chem Co Ltd Preparation of methoxybenzenediazonium salt

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS615061A (en) * 1984-06-15 1986-01-10 Sumitomo Chem Co Ltd Preparation of methoxybenzenediazonium salt

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