GB806759A - Process for the production of derivatives of 3.5-dioxopyrazolidines - Google Patents
Process for the production of derivatives of 3.5-dioxopyrazolidinesInfo
- Publication number
- GB806759A GB806759A GB28083/56A GB2808356A GB806759A GB 806759 A GB806759 A GB 806759A GB 28083/56 A GB28083/56 A GB 28083/56A GB 2808356 A GB2808356 A GB 2808356A GB 806759 A GB806759 A GB 806759A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dioxopyrazolidine
- butyl
- alcohols
- phenyl
- hydroxy
- 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 4-n-butyl- Chemical group 0.000 abstract 9
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 abstract 1
- PYSGFFTXMUWEOT-UHFFFAOYSA-N 3-(dimethylamino)propan-1-ol Chemical compound CN(C)CCCO PYSGFFTXMUWEOT-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
- 239000007868 Raney catalyst Substances 0.000 abstract 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 abstract 1
- 244000028419 Styrax benzoin Species 0.000 abstract 1
- 235000000126 Styrax benzoin Nutrition 0.000 abstract 1
- 235000008411 Sumatra benzointree Nutrition 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 229960002130 benzoin Drugs 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 125000006226 butoxyethyl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- QILSFLSDHQAZET-UHFFFAOYSA-N diphenylmethanol Chemical compound C=1C=CC=CC=1C(O)C1=CC=CC=C1 QILSFLSDHQAZET-UHFFFAOYSA-N 0.000 abstract 1
- 235000019382 gum benzoic Nutrition 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 238000005984 hydrogenation reaction Methods 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical class OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
Landscapes
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Abstract
Derivatives of 3 : 5-dioxopyrazolidine, of the general formula <FORM:0806759/IV (b)/1> wherein R represents a primary or secondary hydrocarbon radical containing at least 2 carbon atoms, which may be interrupted by hetero atoms and may be substituted by hydroxy or oxo groups, and Aryl represents an unsubstituted or substituted phenyl radical, are manufactured by reacting the corresponding compounds unsubstituted in the 4-position with an alcohol R-OH in the presence of a hydrogenation catalyst. Examples describe the preparation, from the appropriate starting materials in the presence of spongy nickel catalyst, of 4-n-butyl-, 4-benzyl-, 4-cyclohexyl-, 4-n-hexyl-, 4-ethyl-, 4-isopropyl-, 4-(41-hydroxybutyl)-, 4-n-dodecyl- and 4-octadecyl-1 : 2-diphenyl - 3 : 5 - dioxopyrazolidine, and of 1 - (p - hydroxy- and p-benzyloxy-phenyl)-2-phenyl-4 - n - butyl - 3 : 5 - dioxopyrazolidine. Additional alcohols specified are n-propyl, isobutyl, sec.-butyl, n-amyl, isoamyl, b -ethylhexyl, hexadecyl, b -phenylethyl, g -phenylpropyl and cinnamyl alcohols, benzhydrol, methoxyethyl, butoxyethyl and ethoxyethoxyethyl alcohols, ethylene, propylene and trimethylene glycols, 1 : 3-butanediol, butanol-4-one-2, benzoin, dimethylaminopropanol and diethylaminoethanol. Reference has been directed by the Comptroller to Specifications 727,405, 773,022, 775,925, 781,438 and 781,439.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH806759X | 1955-09-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB806759A true GB806759A (en) | 1958-12-31 |
Family
ID=4538135
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB28083/56A Expired GB806759A (en) | 1955-09-16 | 1956-09-14 | Process for the production of derivatives of 3.5-dioxopyrazolidines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB806759A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3133933A (en) * | 1964-05-19 | Certain | ||
US3184470A (en) * | 1960-07-20 | 1965-05-18 | Hoechst Ag | New triazolidines |
-
1956
- 1956-09-14 GB GB28083/56A patent/GB806759A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3133933A (en) * | 1964-05-19 | Certain | ||
US3184470A (en) * | 1960-07-20 | 1965-05-18 | Hoechst Ag | New triazolidines |
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