GB738359A - Improvements in or relating to the preparation of aromatic hydroxy carboxylic acids and salts thereof - Google Patents
Improvements in or relating to the preparation of aromatic hydroxy carboxylic acids and salts thereofInfo
- Publication number
- GB738359A GB738359A GB2941053A GB2941053A GB738359A GB 738359 A GB738359 A GB 738359A GB 2941053 A GB2941053 A GB 2941053A GB 2941053 A GB2941053 A GB 2941053A GB 738359 A GB738359 A GB 738359A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkali metal
- aromatic hydroxy
- neutral
- added
- carboxylate
- 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.)
- Expired
Links
- -1 aromatic hydroxy carboxylic acids Chemical class 0.000 title abstract 8
- 150000003839 salts Chemical class 0.000 title abstract 2
- 229910052783 alkali metal Inorganic materials 0.000 abstract 9
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 abstract 9
- 125000003118 aryl group Chemical group 0.000 abstract 8
- 230000007935 neutral effect Effects 0.000 abstract 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 5
- 150000001340 alkali metals Chemical class 0.000 abstract 4
- 238000006243 chemical reaction Methods 0.000 abstract 4
- 238000000034 method Methods 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 150000002989 phenols Chemical class 0.000 abstract 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 abstract 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 abstract 2
- 230000002378 acidificating effect Effects 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 abstract 1
- QPKNFEVLZVJGBM-UHFFFAOYSA-N 2-aminonaphthalen-1-ol Chemical class C1=CC=CC2=C(O)C(N)=CC=C21 QPKNFEVLZVJGBM-UHFFFAOYSA-N 0.000 abstract 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 abstract 1
- MUCCHGOWMZTLHK-UHFFFAOYSA-N 2-nitronaphthalen-1-ol Chemical class C1=CC=C2C(O)=C([N+]([O-])=O)C=CC2=C1 MUCCHGOWMZTLHK-UHFFFAOYSA-N 0.000 abstract 1
- HJSPWKGEPDZNLK-UHFFFAOYSA-N 4-benzylphenol Chemical compound C1=CC(O)=CC=C1CC1=CC=CC=C1 HJSPWKGEPDZNLK-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 150000001339 alkali metal compounds Chemical class 0.000 abstract 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 abstract 1
- 230000002152 alkylating effect Effects 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- 229950011260 betanaphthol Drugs 0.000 abstract 1
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 abstract 1
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical group C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000001569 carbon dioxide Substances 0.000 abstract 1
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000007942 carboxylates Chemical class 0.000 abstract 1
- 230000021523 carboxylation Effects 0.000 abstract 1
- 238000006473 carboxylation reaction Methods 0.000 abstract 1
- 150000001735 carboxylic acids Chemical group 0.000 abstract 1
- 150000001896 cresols Chemical class 0.000 abstract 1
- 150000001908 cumenes Chemical class 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- 125000001033 ether group Chemical group 0.000 abstract 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical group 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 150000004780 naphthols Chemical class 0.000 abstract 1
- RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 1
- 150000003738 xylenes Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/15—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction of organic compounds with carbon dioxide, e.g. Kolbe-Schmitt synthesis
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL191708D NL191708A (enExample) | 1953-10-23 | ||
| NL86578D NL86578C (enExample) | 1953-10-23 | ||
| GB2941053A GB738359A (en) | 1953-10-23 | 1953-10-23 | Improvements in or relating to the preparation of aromatic hydroxy carboxylic acids and salts thereof |
| DES41299A DE1058066B (de) | 1953-10-23 | 1954-10-21 | Verfahren zur Herstellung von Alkalisalzen von Alkylsalicylsaeuren |
| FR1113859D FR1113859A (fr) | 1953-10-23 | 1954-10-21 | Procédé pour la préparation d'acides hydroxycarboniques aromatiques et de sels de ces acides |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2941053A GB738359A (en) | 1953-10-23 | 1953-10-23 | Improvements in or relating to the preparation of aromatic hydroxy carboxylic acids and salts thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB738359A true GB738359A (en) | 1955-10-12 |
Family
ID=10291147
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2941053A Expired GB738359A (en) | 1953-10-23 | 1953-10-23 | Improvements in or relating to the preparation of aromatic hydroxy carboxylic acids and salts thereof |
Country Status (4)
| Country | Link |
|---|---|
| DE (1) | DE1058066B (enExample) |
| FR (1) | FR1113859A (enExample) |
| GB (1) | GB738359A (enExample) |
| NL (2) | NL191708A (enExample) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3448145A (en) * | 1964-09-02 | 1969-06-03 | Alpine Chemische Ag | Process for the production of 2,5-dihydroxyterephthalic acid |
| DE2926694A1 (de) * | 1979-07-02 | 1981-01-29 | Dow Chemical Co | Carbonisierung von alkalimetallphenaten |
| EP0186629A3 (en) * | 1984-12-24 | 1987-06-24 | Ciba-Geigy Ag | Process for the preparation of 3,5-dialkyl-4-hydroxybenzoic acid |
| US4730083A (en) * | 1984-12-24 | 1988-03-08 | Ciba-Geigy Corporation | Process for the preparation of 3,5-dialkyl-4-hydroxy benzoic acid |
| EP0373619A3 (en) * | 1988-12-14 | 1991-11-06 | Kawasaki Steel Corporation | Process for preparing para-hydroxybenzoic acid |
| EP2308953A1 (en) | 2009-09-29 | 2011-04-13 | Chevron Oronite Technology B.V. | System oil formulation for marine two-stroke engines containing alkyl salicylates |
| EP2322591A1 (en) | 2005-07-29 | 2011-05-18 | Chevron Oronite S.A. | Overbased alkaline earth metal alkylhydroxybenzoates having low crude sediment |
| US7951760B2 (en) | 2005-07-29 | 2011-05-31 | Chevron Oronite S.A. | Overbased alkali metal alkylhydroxybenzoates having low crude sediment |
| US8188020B2 (en) | 2003-12-22 | 2012-05-29 | Chevron Oronite S.A. | Lubricating oil composition containing an alkali metal detergent |
| US8618029B2 (en) | 2003-12-22 | 2013-12-31 | Chevron Oronite S.A. | Overbased detergents for lubricating oil applications |
| US8778856B2 (en) | 2009-12-02 | 2014-07-15 | Chevron Oronite Company Llc | Low temperature performance lubricating oil detergents and method of making the same |
| US8993499B2 (en) | 2007-12-28 | 2015-03-31 | Chevron Oronite Company Llc | Low temperature performance lubricating oil detergents and method of making the same |
| CN119118825A (zh) * | 2024-09-10 | 2024-12-13 | 大连理工大学 | 一种光催化γ-羟基羧酸化合物的制备方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2132356A (en) * | 1937-04-29 | 1938-10-04 | Calco Chemical Co Inc | Carboxylation of alkali metal salts of phenols |
| DE817758C (de) * | 1948-04-05 | 1951-10-18 | Eric Berkeley Dr Higgins | Verfahren zur Herstellung des Dinatriumsalzes der 2-Oxynaphthalin-1-carbonsaeure |
-
0
- NL NL86578D patent/NL86578C/xx active
- NL NL191708D patent/NL191708A/xx unknown
-
1953
- 1953-10-23 GB GB2941053A patent/GB738359A/en not_active Expired
-
1954
- 1954-10-21 DE DES41299A patent/DE1058066B/de active Pending
- 1954-10-21 FR FR1113859D patent/FR1113859A/fr not_active Expired
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3448145A (en) * | 1964-09-02 | 1969-06-03 | Alpine Chemische Ag | Process for the production of 2,5-dihydroxyterephthalic acid |
| DE2926694A1 (de) * | 1979-07-02 | 1981-01-29 | Dow Chemical Co | Carbonisierung von alkalimetallphenaten |
| EP0186629A3 (en) * | 1984-12-24 | 1987-06-24 | Ciba-Geigy Ag | Process for the preparation of 3,5-dialkyl-4-hydroxybenzoic acid |
| US4730083A (en) * | 1984-12-24 | 1988-03-08 | Ciba-Geigy Corporation | Process for the preparation of 3,5-dialkyl-4-hydroxy benzoic acid |
| EP0373619A3 (en) * | 1988-12-14 | 1991-11-06 | Kawasaki Steel Corporation | Process for preparing para-hydroxybenzoic acid |
| US5124477A (en) * | 1988-12-14 | 1992-06-23 | Kawasaki Steel Corporation | Process for preparing para-hydroxybenzoic acid |
| US8618029B2 (en) | 2003-12-22 | 2013-12-31 | Chevron Oronite S.A. | Overbased detergents for lubricating oil applications |
| US8188020B2 (en) | 2003-12-22 | 2012-05-29 | Chevron Oronite S.A. | Lubricating oil composition containing an alkali metal detergent |
| US7951760B2 (en) | 2005-07-29 | 2011-05-31 | Chevron Oronite S.A. | Overbased alkali metal alkylhydroxybenzoates having low crude sediment |
| EP2322591A1 (en) | 2005-07-29 | 2011-05-18 | Chevron Oronite S.A. | Overbased alkaline earth metal alkylhydroxybenzoates having low crude sediment |
| US8993499B2 (en) | 2007-12-28 | 2015-03-31 | Chevron Oronite Company Llc | Low temperature performance lubricating oil detergents and method of making the same |
| US8383562B2 (en) | 2009-09-29 | 2013-02-26 | Chevron Oronite Technology B.V. | System oil formulation for marine two-stroke engines |
| EP2308953A1 (en) | 2009-09-29 | 2011-04-13 | Chevron Oronite Technology B.V. | System oil formulation for marine two-stroke engines containing alkyl salicylates |
| US8778856B2 (en) | 2009-12-02 | 2014-07-15 | Chevron Oronite Company Llc | Low temperature performance lubricating oil detergents and method of making the same |
| CN119118825A (zh) * | 2024-09-10 | 2024-12-13 | 大连理工大学 | 一种光催化γ-羟基羧酸化合物的制备方法 |
| CN119118825B (zh) * | 2024-09-10 | 2025-12-02 | 大连理工大学 | 一种光催化γ-羟基羧酸化合物的制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1113859A (fr) | 1956-04-05 |
| DE1058066B (de) | 1959-05-27 |
| NL86578C (enExample) | |
| NL191708A (enExample) |
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