GB672104A - Improvements in or relating to esters of 2,4-dichlorophenoxy acetic acid - Google Patents
Improvements in or relating to esters of 2,4-dichlorophenoxy acetic acidInfo
- Publication number
- GB672104A GB672104A GB1397650A GB1397650A GB672104A GB 672104 A GB672104 A GB 672104A GB 1397650 A GB1397650 A GB 1397650A GB 1397650 A GB1397650 A GB 1397650A GB 672104 A GB672104 A GB 672104A
- Authority
- GB
- United Kingdom
- Prior art keywords
- propanol
- propoxy
- esters
- acid
- relating
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
- C07C69/708—Ethers
- C07C69/712—Ethers the hydroxy group of the ester being etherified with a hydroxy compound having the hydroxy group bound to a carbon atom of a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Esters of 2 : 4-dichlorophenoxyacetic acid in which the ester group is an alkyl (1-4 C) monoether of mono-dipropylene glycol are obtained by condensing the acid with at least one molecular proportion of the glycol alkyl monoether in presence of dehydration catalysts, if desired in presence of a water-immiscible solvent. In examples, 2 : 4-dichlorophenoxyacetic acid is condensed with propoxy-propoxypropanol, 1 - butoxy - 2 - propanol, butoxy - propoxy-propanol, 1-isopropoxy and 1-propoxy-2-propanol, and 2-methoxy-1-propanol, to give the corresponding esters. Other etherifying alcohol-ethers specified include:-ethoxy-propanol, propoxy-propanol, methoxy-propoxypropanol, and ethoxy-propoxy-propanol; glycol alkyl ethers employed as above are obtained by reaction of propylene oxide with an aliphatic alcohol in presence of an acid or alkaline catalyst.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1397650A GB672104A (en) | 1950-06-05 | 1950-06-05 | Improvements in or relating to esters of 2,4-dichlorophenoxy acetic acid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1397650A GB672104A (en) | 1950-06-05 | 1950-06-05 | Improvements in or relating to esters of 2,4-dichlorophenoxy acetic acid |
Publications (1)
Publication Number | Publication Date |
---|---|
GB672104A true GB672104A (en) | 1952-05-14 |
Family
ID=10032778
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1397650A Expired GB672104A (en) | 1950-06-05 | 1950-06-05 | Improvements in or relating to esters of 2,4-dichlorophenoxy acetic acid |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB672104A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2119685A1 (en) * | 1996-06-18 | 1998-10-01 | Consejo Superior De Investiaga | Process for obtaining 2,4-dichlorophenoxyacetic acid (2,4- D) in the dry phase |
-
1950
- 1950-06-05 GB GB1397650A patent/GB672104A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2119685A1 (en) * | 1996-06-18 | 1998-10-01 | Consejo Superior De Investiaga | Process for obtaining 2,4-dichlorophenoxyacetic acid (2,4- D) in the dry phase |
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