JPS6422832A - Purification of high-purity 2,4-xylenol - Google Patents

Purification of high-purity 2,4-xylenol

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Publication number
JPS6422832A
JPS6422832A JP17727887A JP17727887A JPS6422832A JP S6422832 A JPS6422832 A JP S6422832A JP 17727887 A JP17727887 A JP 17727887A JP 17727887 A JP17727887 A JP 17727887A JP S6422832 A JPS6422832 A JP S6422832A
Authority
JP
Japan
Prior art keywords
xylenol
aldehyde
isomer mixture
purify
purity
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
JP17727887A
Other languages
Japanese (ja)
Inventor
Toru Miura
Katsuji Watanabe
Hitoshi Nakayama
Masayuki Furuya
Teruyuki Nagata
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 JP17727887A priority Critical patent/JPS6422832A/en
Publication of JPS6422832A publication Critical patent/JPS6422832A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To purify the titled high-purity compound, by reacting a xylenol isomer mixture with an aldehyde and while severely controlling consumption of a mineral acid used in condensed reaction and condensation reaction temperature and separating and removing 2,5-xylenol as a condensed product. CONSTITUTION:A xylenol isomer mixture (preferably crude 2,4-xylenol, especially containing 85-95% 2,4-xylenol) containing 2,4-xylenol and 2,5-xylenol is reacted with an aldehyde in the presence of a mineral acid (especially preferably hydrochloric acid or sulfuric acid) of 0.01-2pts.wt., especially 0.10-0.20pt.wt. based on 100pts.wt. xylenol isomer mixture at 0-50 deg.C (especially preferably 10-30 deg.C) to afford 2,5-xylenol as a xylenolaldehyde condensation product, which is then separated from 2,4-xylenol to purify 2,4-xylenol. 0.5-1.5 time mol. aldehyde is preferably used to 1mol. 2,5-xylenol.
JP17727887A 1987-07-17 1987-07-17 Purification of high-purity 2,4-xylenol Pending JPS6422832A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17727887A JPS6422832A (en) 1987-07-17 1987-07-17 Purification of high-purity 2,4-xylenol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17727887A JPS6422832A (en) 1987-07-17 1987-07-17 Purification of high-purity 2,4-xylenol

Publications (1)

Publication Number Publication Date
JPS6422832A true JPS6422832A (en) 1989-01-25

Family

ID=16028250

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17727887A Pending JPS6422832A (en) 1987-07-17 1987-07-17 Purification of high-purity 2,4-xylenol

Country Status (1)

Country Link
JP (1) JPS6422832A (en)

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