BE436362A - - Google Patents
Info
- Publication number
- BE436362A BE436362A BE436362DA BE436362A BE 436362 A BE436362 A BE 436362A BE 436362D A BE436362D A BE 436362DA BE 436362 A BE436362 A BE 436362A
- Authority
- BE
- Belgium
- Prior art keywords
- obtains
- compound
- parts
- residue
- reduction
- Prior art date
Links
- 239000003638 chemical reducing agent Substances 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 241001585714 Nola Species 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- UCTWMZQNUQWSLP-UHFFFAOYSA-N adrenaline Chemical compound CNCC(O)C1=CC=C(O)C(O)=C1 UCTWMZQNUQWSLP-UHFFFAOYSA-N 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- OTHYPAMNTUGKDK-UHFFFAOYSA-N (3-acetylphenyl) acetate Chemical compound CC(=O)OC1=CC=CC(C(C)=O)=C1 OTHYPAMNTUGKDK-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- MOIPGXQKZSZOQX-UHFFFAOYSA-N carbonyl bromide Chemical compound BrC(Br)=O MOIPGXQKZSZOQX-UHFFFAOYSA-N 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE436362A true BE436362A (en:Method) |
Family
ID=95044
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE436362D BE436362A (en:Method) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE436362A (en:Method) |
-
0
- BE BE436362D patent/BE436362A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| BE436362A (en:Method) | ||
| FR2807427A1 (fr) | Plastifiant energetique comprenant un melange eutectique de bis (2,2-dinitropropyl) formal, de 2,2 dinitropropyl- 2,2-dinitrobutylformal et de bis (2,2-dinitrobutyl) formal, et son procede de preparation | |
| JP2835313B2 (ja) | イオパミドールの精製及び晶出方法 | |
| BE660217A (en:Method) | ||
| BE378351A (en:Method) | ||
| CA1186327A (fr) | PROCEDE AMELIORE DE FABRICATION DE L'.alpha.-ACETOXY-.alpha.- METHYL N,N'-DIACETYL MALONAMIDE DE HAUTE PRODUCTIVITE | |
| CH400121A (fr) | Procédé de préparation de nouveaux dérivés de l'héparine | |
| BE500594A (en:Method) | ||
| BE528076A (en:Method) | ||
| BE569139A (en:Method) | ||
| BE432776A (en:Method) | ||
| BE573277A (en:Method) | ||
| BE499168A (en:Method) | ||
| BE527112A (en:Method) | ||
| CH290796A (fr) | Procédé de préparation d'un amino-alcool tertiaire. | |
| BE429362A (en:Method) | ||
| BE436984A (en:Method) | ||
| FR2558465A1 (fr) | Procede de preparation d'un derive de benzamide et derive ainsi obtenu | |
| CH93814A (fr) | Procédé pour la fabrication d'un acétate de cellulose. | |
| BE523986A (en:Method) | ||
| BE635463A (en:Method) | ||
| BE417716A (en:Method) | ||
| BE520758A (en:Method) | ||
| CH330821A (fr) | Procédé de dédoublement de la DL-sérine | |
| BE497366A (en:Method) |