BE634177A - - Google Patents
Info
- Publication number
- BE634177A BE634177A BE634177DA BE634177A BE 634177 A BE634177 A BE 634177A BE 634177D A BE634177D A BE 634177DA BE 634177 A BE634177 A BE 634177A
- Authority
- BE
- Belgium
- Prior art keywords
- compound
- alpha
- hydroxyl group
- hydrogenation
- hydrogen
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 238000005984 hydrogenation reaction Methods 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 241001024304 Mino Species 0.000 claims 1
- 229940060587 alpha e Drugs 0.000 claims 1
- RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 3
- YQRDADVUUPKUBC-UHFFFAOYSA-N 2-methyl-n-phenylbutanamide Chemical compound CCC(C)C(=O)NC1=CC=CC=C1 YQRDADVUUPKUBC-UHFFFAOYSA-N 0.000 description 2
- -1 aminopropionyl Chemical group 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- MXZROAOUCUVNHX-UHFFFAOYSA-N 2-Aminopropanol Chemical class CCC(N)O MXZROAOUCUVNHX-UHFFFAOYSA-N 0.000 description 1
- ILLHORFDXDLILE-UHFFFAOYSA-N 2-bromopropanoyl bromide Chemical compound CC(Br)C(Br)=O ILLHORFDXDLILE-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000003589 local anesthetic agent Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE634177A true BE634177A (enrdf_load_html_response) |
Family
ID=201364
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE634177D BE634177A (enrdf_load_html_response) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE634177A (enrdf_load_html_response) |
-
0
- BE BE634177D patent/BE634177A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BE1006426A6 (fr) | Procede de preparation de la n-methyl-3-phenyl-3-[4-(trifluoromethyl)-phenoxy]-propylamine et de ses sels d'addition d'acide. | |
BE462272A (fr) | Procédé de préparation de composés chimiques | |
BE634177A (enrdf_load_html_response) | ||
EP0003460A1 (fr) | Préparation du tris (hydroxyméthyl) aminométhane | |
FR2701946A1 (fr) | Procédé pour la préparation d'un aminoalcool optiquement pur. | |
EP0385835A1 (fr) | Procédé de préparation de n-allylmetatrifluoromethylaniline | |
FR2467842A1 (fr) | Procede pour la production d'iminodiacetonitrile | |
FR2615853A1 (fr) | Nouveau procede pour la preparation de derives de la piperazine pharmacologiquement actifs, derives et nouveaux intermediaires obtenus | |
BE361696A (enrdf_load_html_response) | ||
BE721233A (enrdf_load_html_response) | ||
US8168833B2 (en) | Schwartz reagents: methods of in situ generation and use | |
WO2024040111A1 (en) | Process for the preparation and isolation of intermediates of certain mesoionic pesticides | |
FR2494696A1 (fr) | Nouveau procede de preparation de steroides 3-amines et leurs sels | |
BE477026A (enrdf_load_html_response) | ||
BE519855A (enrdf_load_html_response) | ||
BE631288A (enrdf_load_html_response) | ||
BE554056A (enrdf_load_html_response) | ||
BE555876A (enrdf_load_html_response) | ||
JPS63196555A (ja) | ヒドロキシベンズアルドキシムo−エーテルの製造方法 | |
JPS63218637A (ja) | cis−クロチルアルコ−ルの製造法 | |
BE538254A (enrdf_load_html_response) | ||
BE550990A (enrdf_load_html_response) | ||
BE485370A (enrdf_load_html_response) | ||
BE529283A (enrdf_load_html_response) | ||
BE859838A (fr) | Hydrogenation de composes bis (cyano-2 ethoxy) |