NL7712270A - Methyl-di:tert.-butyl:phenol purification - by crystallisation from aq. methanol at low temp. - Google Patents
Methyl-di:tert.-butyl:phenol purification - by crystallisation from aq. methanol at low temp.Info
- Publication number
- NL7712270A NL7712270A NL7712270A NL7712270A NL7712270A NL 7712270 A NL7712270 A NL 7712270A NL 7712270 A NL7712270 A NL 7712270A NL 7712270 A NL7712270 A NL 7712270A NL 7712270 A NL7712270 A NL 7712270A
- Authority
- NL
- Netherlands
- Prior art keywords
- methanol
- butyl
- prod
- methyl
- butylphenol
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/68—Purification; separation; Use of additives, e.g. for stabilisation
- C07C37/70—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment
- C07C37/84—Purification; separation; Use of additives, e.g. for stabilisation by physical treatment by crystallisation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Purificn. of 4-methyl-2,6-di-t-butylphenol (I) comprises crystallising at 0-5 degrees C from methanol contg. 3-10 w/w % of water, the ratio of solute to aq. methanol ranging from 1:1 to 1:4. The prod. is made by O-alkylation of phenol then aminomethylation and hydrogenolysis of the resultant N,N-dimethyl-3,5-di-ti-butyl-4-hydroxybenzylamine. Aq. methanol containing 3% of water leads to increased losses of prod. The prod. is a colourless stabiliser for synthetic rubber and polymers, an antioxidant for oils, fuels and other petroleum prods. as stabiliser in foods and drugs. The process removes impurities such as 2,6-di-t-butylphenol 2,4,6-tri-t-butylphenol and 2,6-di-ti-butyl-4-methylcyclohexanone with reduced losses of the desired prod. which is obtd. at a purity of =99.95%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL7712270A NL7712270A (en) | 1977-11-08 | 1977-11-08 | Methyl-di:tert.-butyl:phenol purification - by crystallisation from aq. methanol at low temp. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL7712270A NL7712270A (en) | 1977-11-08 | 1977-11-08 | Methyl-di:tert.-butyl:phenol purification - by crystallisation from aq. methanol at low temp. |
Publications (1)
Publication Number | Publication Date |
---|---|
NL7712270A true NL7712270A (en) | 1979-05-10 |
Family
ID=19829492
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NL7712270A NL7712270A (en) | 1977-11-08 | 1977-11-08 | Methyl-di:tert.-butyl:phenol purification - by crystallisation from aq. methanol at low temp. |
Country Status (1)
Country | Link |
---|---|
NL (1) | NL7712270A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7355082B2 (en) * | 2001-04-23 | 2008-04-08 | Basf Aktiengesellschaft | Method of purifying long-chain alkyl phenols and Mannich adducts thereof |
-
1977
- 1977-11-08 NL NL7712270A patent/NL7712270A/en not_active Application Discontinuation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7355082B2 (en) * | 2001-04-23 | 2008-04-08 | Basf Aktiengesellschaft | Method of purifying long-chain alkyl phenols and Mannich adducts thereof |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
A1C | A request for examination has been filed | ||
BI | The patent application has been withdrawn |