JPS57188535A - Preparation of p-cumylphenol - Google Patents
Preparation of p-cumylphenolInfo
- Publication number
- JPS57188535A JPS57188535A JP56073578A JP7357881A JPS57188535A JP S57188535 A JPS57188535 A JP S57188535A JP 56073578 A JP56073578 A JP 56073578A JP 7357881 A JP7357881 A JP 7357881A JP S57188535 A JPS57188535 A JP S57188535A
- Authority
- JP
- Japan
- Prior art keywords
- methylstyrene
- catalyst
- exchange resin
- cation exchange
- suspension
- 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
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
PURPOSE: To obtain the titled substance continuously in high yield, by reacting phenol with α-methylstyrene in a given molar ratio in a reactor of the complete blending type in a suspension of a catalyst of cation exchange resin for a constant retention time.
CONSTITUTION: Phenol is reacted with α-methylstyrene in a molr ratio of ≥1.0 (preferably 2.5W3.5) in a container of the complete blending type in a suspension of a cation exchange resin catalyst for 10minW2hr (preferably 30W60min), to give the titled substance. A strong acidic cation exchange resin such as Lewatit SPC 118H, Amberlyst 15, etc. may be cited as the catalyst, and its amount to be fed per hour is 5W15wt% based on α-methylstyrene. The reaction temperature is preferably 90W110°C.
EFFECT: Dimerization of α-methylstyrene and preparation of o-cumylphenol as a by-product are suppressed.
USE: Germicide. A raw material for surface active agents, antioxidants, resins, etc.
COPYRIGHT: (C)1982,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56073578A JPS57188535A (en) | 1981-05-18 | 1981-05-18 | Preparation of p-cumylphenol |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56073578A JPS57188535A (en) | 1981-05-18 | 1981-05-18 | Preparation of p-cumylphenol |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS57188535A true JPS57188535A (en) | 1982-11-19 |
Family
ID=13522310
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56073578A Pending JPS57188535A (en) | 1981-05-18 | 1981-05-18 | Preparation of p-cumylphenol |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57188535A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5043483A (en) * | 1987-12-01 | 1991-08-27 | Montedison S.P.A. | Process for the alkylation of phenols |
US5091058A (en) * | 1990-02-20 | 1992-02-25 | Aristech Chemical Corporation | Purified para-cumylphenol |
US5185475A (en) * | 1992-06-01 | 1993-02-09 | General Electric Company | Process for preparing paracumylphenol |
US5235116A (en) * | 1992-08-24 | 1993-08-10 | Eastman Kodak Company | Process for the preparation of 2-(1-phenylethyl)hydroquinone and 2-(1-phenylethyl)hydroquinone diacetate |
US5608120A (en) * | 1988-05-31 | 1997-03-04 | Granmont, Inc. | Process for the preparation of (arylethyl)-hydroquinones and diesters thereof |
CN115636731A (en) * | 2022-10-14 | 2023-01-24 | 宿迁联盛科技股份有限公司 | Synthesis method of 2, 4-dicumylphenol |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4832851A (en) * | 1971-08-10 | 1973-05-02 | ||
JPS5019742A (en) * | 1973-06-18 | 1975-03-01 |
-
1981
- 1981-05-18 JP JP56073578A patent/JPS57188535A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4832851A (en) * | 1971-08-10 | 1973-05-02 | ||
JPS5019742A (en) * | 1973-06-18 | 1975-03-01 |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5043483A (en) * | 1987-12-01 | 1991-08-27 | Montedison S.P.A. | Process for the alkylation of phenols |
US5608120A (en) * | 1988-05-31 | 1997-03-04 | Granmont, Inc. | Process for the preparation of (arylethyl)-hydroquinones and diesters thereof |
US5091058A (en) * | 1990-02-20 | 1992-02-25 | Aristech Chemical Corporation | Purified para-cumylphenol |
US5185475A (en) * | 1992-06-01 | 1993-02-09 | General Electric Company | Process for preparing paracumylphenol |
US5235116A (en) * | 1992-08-24 | 1993-08-10 | Eastman Kodak Company | Process for the preparation of 2-(1-phenylethyl)hydroquinone and 2-(1-phenylethyl)hydroquinone diacetate |
CN115636731A (en) * | 2022-10-14 | 2023-01-24 | 宿迁联盛科技股份有限公司 | Synthesis method of 2, 4-dicumylphenol |
CN115636731B (en) * | 2022-10-14 | 2024-04-09 | 宿迁联盛科技股份有限公司 | Synthesis method of 2, 4-dicumyl phenol |
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