GB1493605A - Preparation of aminophenylalkyl ethers - Google Patents
Preparation of aminophenylalkyl ethersInfo
- Publication number
- GB1493605A GB1493605A GB4652674A GB4652674A GB1493605A GB 1493605 A GB1493605 A GB 1493605A GB 4652674 A GB4652674 A GB 4652674A GB 4652674 A GB4652674 A GB 4652674A GB 1493605 A GB1493605 A GB 1493605A
- Authority
- GB
- United Kingdom
- Prior art keywords
- preparation
- dipotassium
- disodium
- diborate
- moieties
- 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
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/02—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
1493605 Preparation of aminophenylalkylethers HOECHST AG 28 Oct 1974 [30 Oct 1973] 46526/74 Addition to 1323440 Heading C2C A process for the preparation of an aminophenyl alkyl ether of formula wherein z represents 0 or an integer from 1 to 3, each of the Y moieties, any two or more of which may be the same or different represents a C 1-4 alkyl group, n represents an integer from 1 to 3, and each of the X moieties, any two or more of which may be the same or different represents a C 1-4 alkyl group, comprises catalytically hydrogenating the corresponding nitroderivatives in the presence of (i) an inert aromatic hydrocarbon which has a dielectric constant in the range of from 2 to 3 and which under the reaction conditions is immiscible with water but capable of dissolving the starting material and amino end product, e.g. benzene, toluene, isomeric xylenes, ethylbenzene and cumene; (ii) an inorganic salt which maintains a pH in the range of from 8 to 10 during the reaction. The preferred inorganic salts are disodium hydrogen phosphate, disodium tetraborate, disodium diborate, sodium acetate, sodium formate or dipotassium hydrogen phosphate, dipotassium tetraborate, dipotassium diborate, potassium acetate or potassium formate. The following compounds are prepared in the examples: resorcinol dimethyl ether, o- and p-anisidine and aminohydroquinonedimethylether.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19732354288 DE2354288C2 (en) | 1973-10-30 | 1973-10-30 | Process for the preparation of aminophenylalkyl ethers |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1493605A true GB1493605A (en) | 1977-11-30 |
Family
ID=5896833
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4652674A Expired GB1493605A (en) | 1973-10-30 | 1974-10-28 | Preparation of aminophenylalkyl ethers |
Country Status (9)
Country | Link |
---|---|
JP (1) | JPS5126833A (en) |
BE (1) | BE821683R (en) |
CA (1) | CA1040657A (en) |
CH (1) | CH574392A5 (en) |
DE (1) | DE2354288C2 (en) |
FR (1) | FR2249072B1 (en) |
GB (1) | GB1493605A (en) |
IT (1) | IT1046401B (en) |
NL (1) | NL7413992A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IE980216A1 (en) * | 1989-04-17 | 2000-02-23 | Scotia Holdings Plc | Anti-virals |
US20030162230A1 (en) | 2000-09-27 | 2003-08-28 | Reagan Kevin J. | Method for quantifying phosphokinase activity on proteins |
-
1973
- 1973-10-30 DE DE19732354288 patent/DE2354288C2/en not_active Expired
-
1974
- 1974-10-25 NL NL7413992A patent/NL7413992A/en not_active Application Discontinuation
- 1974-10-25 CH CH1436474A patent/CH574392A5/xx not_active IP Right Cessation
- 1974-10-28 IT IT2888474A patent/IT1046401B/en active
- 1974-10-28 GB GB4652674A patent/GB1493605A/en not_active Expired
- 1974-10-29 JP JP12400674A patent/JPS5126833A/en active Pending
- 1974-10-29 CA CA212,489A patent/CA1040657A/en not_active Expired
- 1974-10-30 FR FR7436283A patent/FR2249072B1/fr not_active Expired
- 1974-10-30 BE BE150060A patent/BE821683R/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
FR2249072A1 (en) | 1975-05-23 |
DE2354288B1 (en) | 1975-03-20 |
IT1046401B (en) | 1980-06-30 |
CA1040657A (en) | 1978-10-17 |
BE821683R (en) | 1975-04-30 |
JPS5126833A (en) | 1976-03-05 |
DE2354288C2 (en) | 1976-01-02 |
CH574392A5 (en) | 1976-04-15 |
NL7413992A (en) | 1975-05-02 |
FR2249072B1 (en) | 1978-06-09 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |