GB292615A - - Google Patents
Info
- Publication number
- GB292615A GB292615A GB18191/28A GB1819128A GB292615A GB 292615 A GB292615 A GB 292615A GB 18191/28 A GB18191/28 A GB 18191/28A GB 1819128 A GB1819128 A GB 1819128A GB 292615 A GB292615 A GB 292615A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alpha
- product
- gamma
- chloride
- amino group
- 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 Aliphatic diamines Chemical class 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- YMDNODNLFSHHCV-UHFFFAOYSA-N 2-chloro-n,n-diethylethanamine Chemical compound CCN(CC)CCCl YMDNODNLFSHHCV-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- 125000003277 amino group Chemical group 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 239000003814 drug Substances 0.000 abstract 2
- 229940079593 drug Drugs 0.000 abstract 2
- 150000003336 secondary aromatic amines Chemical class 0.000 abstract 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 abstract 2
- OVOWTANBDBUKBN-UHFFFAOYSA-N 1-chloro-n,n-dimethylbutan-1-amine Chemical compound CCCC(Cl)N(C)C OVOWTANBDBUKBN-UHFFFAOYSA-N 0.000 abstract 1
- MRLYNABCKVRNFY-UHFFFAOYSA-N 1-n,1-n,3-n-trimethylbutane-1,3-diamine Chemical compound CNC(C)CCN(C)C MRLYNABCKVRNFY-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 abstract 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 125000003968 arylidene group Chemical group [H]C(c)=* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- GUZZRZFJWKNPHZ-UHFFFAOYSA-N n',n'-diethyl-n-methyl-n-phenylethane-1,2-diamine Chemical compound CCN(CC)CCN(C)C1=CC=CC=C1 GUZZRZFJWKNPHZ-UHFFFAOYSA-N 0.000 abstract 1
- QUMIGAREEPSVLG-UHFFFAOYSA-N n',n'-diethyl-n-phenylethane-1,2-diamine Chemical compound CCN(CC)CCNC1=CC=CC=C1 QUMIGAREEPSVLG-UHFFFAOYSA-N 0.000 abstract 1
- BXEFFCMWYFJKBI-UHFFFAOYSA-N n,n,n'-triethyl-n'-phenylethane-1,2-diamine Chemical compound CCN(CC)CCN(CC)C1=CC=CC=C1 BXEFFCMWYFJKBI-UHFFFAOYSA-N 0.000 abstract 1
- 150000002832 nitroso derivatives Chemical class 0.000 abstract 1
- MLPVBIWIRCKMJV-UHFFFAOYSA-N o-aminoethylbenzene Natural products CCC1=CC=CC=C1N MLPVBIWIRCKMJV-UHFFFAOYSA-N 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 abstract 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 abstract 1
- 239000004289 sodium hydrogen sulphite Substances 0.000 abstract 1
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 1
- 235000010288 sodium nitrite Nutrition 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 238000006467 substitution reaction Methods 0.000 abstract 1
- 125000001302 tertiary amino group Chemical group 0.000 abstract 1
- 239000011800 void material Substances 0.000 abstract 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE292615T | 1927-06-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB292615A true GB292615A (enrdf_load_stackoverflow) | 1929-07-18 |
Family
ID=31894027
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB18191/28A Expired GB292615A (enrdf_load_stackoverflow) | 1927-06-23 | 1928-06-22 |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB292615A (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2762697A (en) * | 1951-06-23 | 1956-09-11 | Monsanto Chemicals | N-(alkylmercaptoalkyl) polyamine herbicides |
| DE1128861B (de) * | 1958-07-04 | 1962-05-03 | Davis & Company | Verfahren zur Herstellung von Thioxanthonderivaten |
| JP2003514888A (ja) * | 1999-11-25 | 2003-04-22 | ビーエーエスエフ アクチェンゲゼルシャフト | 光学活性アミンの製造方法 |
-
1928
- 1928-06-22 GB GB18191/28A patent/GB292615A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2762697A (en) * | 1951-06-23 | 1956-09-11 | Monsanto Chemicals | N-(alkylmercaptoalkyl) polyamine herbicides |
| DE1128861B (de) * | 1958-07-04 | 1962-05-03 | Davis & Company | Verfahren zur Herstellung von Thioxanthonderivaten |
| JP2003514888A (ja) * | 1999-11-25 | 2003-04-22 | ビーエーエスエフ アクチェンゲゼルシャフト | 光学活性アミンの製造方法 |
| JP4776846B2 (ja) * | 1999-11-25 | 2011-09-21 | ビーエーエスエフ ソシエタス・ヨーロピア | 光学活性アミンの製造方法 |
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