BE510225A - - Google Patents
Info
- Publication number
- BE510225A BE510225A BE510225DA BE510225A BE 510225 A BE510225 A BE 510225A BE 510225D A BE510225D A BE 510225DA BE 510225 A BE510225 A BE 510225A
- Authority
- BE
- Belgium
- Prior art keywords
- solution
- alkali
- propanediol
- nitro
- phenyl
- Prior art date
Links
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 11
- 239000003513 alkali Substances 0.000 claims description 7
- CMWKITSNTDAEDT-UHFFFAOYSA-N 2-nitrobenzaldehyde Chemical compound [O-][N+](=O)C1=CC=CC=C1C=O CMWKITSNTDAEDT-UHFFFAOYSA-N 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- -1 ION sodium hydroxide Chemical class 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- LMRDBJZQDUVCQH-UHFFFAOYSA-N 2-(1,3-dioxoisoindol-2-yl)acetaldehyde Chemical compound C1=CC=C2C(=O)N(CC=O)C(=O)C2=C1 LMRDBJZQDUVCQH-UHFFFAOYSA-N 0.000 claims description 3
- 238000009833 condensation Methods 0.000 claims description 3
- 230000005494 condensation Effects 0.000 claims description 3
- 230000004048 modification Effects 0.000 claims 2
- 238000012986 modification Methods 0.000 claims 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000003518 caustics Substances 0.000 description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000009089 cytolysis Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 125000001145 hydrido group Chemical group *[H] 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical group C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- LMHHRCOWPQNFTF-UHFFFAOYSA-N s-propan-2-yl azepane-1-carbothioate Chemical compound CC(C)SC(=O)N1CCCCCC1 LMHHRCOWPQNFTF-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE510225A true BE510225A (d) |
Family
ID=149409
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE510225D BE510225A (d) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE510225A (d) |
-
0
- BE BE510225D patent/BE510225A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
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 | |
BE510225A (d) | ||
EP3750873B1 (fr) | Procédé de fabrication de n-acétyl-taurinate de magnésium | |
BE466916A (d) | ||
EP0188979A1 (fr) | Procédé de préparation d'anthraquinone | |
CH298379A (fr) | Procédé de préparation de l'allo-1-p-nitrophényl-2-(ortho-carboxybenzoyl)-amino-propanediol-1,3. | |
EP0022041B1 (fr) | Procédé de préparation de benzoxazolone | |
Sauer et al. | Nitramines. I. Methylenedinitramine1 | |
WO1985002404A1 (fr) | Nouveaux derives de peptides, leur procede de preparation et leur emploi comme reactif biologique | |
BE360796A (d) | ||
BE518687A (d) | ||
BE381464A (d) | ||
CH83508A (fr) | Procédé de préparation d'acide picrique par nitration des dinitrophénols | |
BE505594A (d) | ||
CH89373A (fr) | Procédé pour la fabrication de l'aldéhyde acétique en partant de l'acétylène. | |
BE354112A (d) | ||
BE560101A (d) | ||
CH242349A (fr) | Procédé de fabrication d'acétals en présence d'un catalyseur contenant des composés du mercure. | |
BE430699A (d) | ||
BE430582A (d) | ||
BE582878A (d) | ||
BE525639A (d) | ||
BE421682A (d) | ||
BE480661A (d) | ||
BE636819A (d) |